Cyclohexenonoxime ethers and herbicidal composition
Abstract
Cyclohexenone oxime ethers of the formula I <IMAGE> (I) (R1=C1-C6-alkyl; A=substituted or unsubstituted alkylene or alkenylene; Z=a 5-membered or 6-membered heteroaromatic structure; X=substituted or unsubstituted amino, nitro, cyano, halogen, alkyl, C1-C4-alkoxy, C1-C4-alkylthio, C1-C4-haloalkyl, C1-C4-haloalkoxy, carboxyl, C1-C4-alkoxycarbonyl, substituted or unsubstituted benzyloxycarbonyl and phenyl; n=0 to 3, or 1 to 4 where Z is halogen-substituted pyridyl; and R2=alkoxyalkyl or alkylthioalkyl; substituted or unsubstituted cycloalkyl or cycloalkenyl; a substituted or unsubstituted 5-membered saturated heterocyclic structure which contains one or two hetero atoms; a substituted or unsubstituted 6-membered or 7-membered saturated or mono- or diunsaturated heterocyclic structure containing one or two hereto atoms; a substituted or unsubstituted 5-membered heteroaromatic structure containing one to three hereto atoms; substituted or unsubstituted phenyl or pyridyl) and their agriculturally useful salts and esters of C1-C10-carboxylic acids and inorganic acids. The compounds are suitable as herbicides.

Term
Term ended
Expired 6 May 2013, 13.4 years ago.
- Priority
- Filed
- Granted
- Expired
- Today
3 claims: 3 independent, 0 dependent
- 1DEFINITION OF INVENTION IŠRADIMO APIBRĖŽTIS 1. Cyclohexenone oxime ethers of the general formula (I) wherein the substituents have the following meanings:1. Cikloheksenonoksimo eteriai bendros formulės (I), kurioje pakaitai turi tokias reikšmes: alkoksilo, C1-C4-tioalkilo, Cx-C4-halogenalkilo, C1-C4-halogenalkoksilo, karboksilo, alkoxyl, C1-C4-thioalkyl, Cx-C4-haloalkyl, C1-C4-haloalkoxyl, carboxyl, Cx-C4-ai koks ii karbonilo, benziloksikarbonilo, fenilo, be to, aromatiniai radikalai dar gali turėti 1-3 tokius pakaitus: nitro, ciano, halogeno, Cx-C4-alkilo, Cx-C4-alkoksilo, C1-C4tioalkilo, Cx-C4 - halogenalkilo, Cx-C4 halogenalkoksilo, karboksilo, Cx-C4 alkoksilkarbonilo, benziloksikarbonilo;Cx-C4such as carbonyl, benzyloxycarbonyl, phenyl, and aromatic radicals may be further substituted with one to three of the following: nitro, cyano, halogen, Cx-C4-alkyl, Cx-C4-alkoxyl, C1-C4thioalkyl, Cx-C4 - haloalkyl, Cx-C4 haloalkoxyl, carboxyl, Cx-C4 alkoxylcarbonyl, benzyloxycarbonyl;n - 0-3 arba 1-4 tam atvejui, kada Z - halogenu pakeistas piridilo radikalas;n is 0-3 or 1-4 when Z is a halogen substituted pyridyl radical;R2 - Cx-C4 - alkoksilo-Cį-Cg - alkilo - arba Cx-C4 tioalkilo-C^-Cg - alkilo grupė, C3-C7 - cikloalkilo grupė, be to šios grupės dar gali turėti R2 - Cx-C4 - alkoxyl-C 1 -C 8 - alkyl - or Cx-C4 thioalkyl-C 1 -C 8 - alkyl group, C3-C7 - a cycloalkyl group which may additionally be present 1-3 radicals which may contain Cx-C4 - alkyl, Cx-C4 - alkoxyl, Cx-C4 - thioalkyl, Cx-C4 haloalkyl, hydroxy or halogen;1-3 radikalus, kuriais gali būti Cx-C4 - alkilas, Cx-C4 - alkoksilas, Cx-C4 - tioalkilas, Cx-C4 halogenalkilas, hidroksilas arba halogenas;5- naris prisotintas heterociklas, kuris turi 1 ar 2 heteroatomus, kuriais gali būti deguonis ar siera, be to, heterociklas dar gali turėti A 5-membered saturated heterocycle containing 1 or 2 heteroatoms which may be oxygen or sulfur, in addition the heterocycle may have 1-3 radicals of C 1 -C 4 alkyl;Cx-C4 - alkoxyl, Cx-C4 - thioalkyl and Cx-C4 - haloalkyl groups;1-3 radikalus iš Cj-C^ - alkilo;Cx-C4 - alkoksilo, Cx-C4 - tioalkilo ir Cx-C4 - halogenalkilo grupių;6- ar 7-naris prisotintas arba vieną ar du kartus neprisotintas heterociklas, turintis 1 ar A 6- or 7-membered saturated or mono- or double-unsaturated heterocycle containing 1 or
- 22 heteroatoms from the oxygen or sulfur group, and this ring may also contain 1-3 radicals which may be hydroxyl, halogen, Cx-C4 alkyl, Cx-C4 - alkoxyl, Cx-C4 - thioalkyl and Cx-C4 - haloalkyl;2 heteroatomus iš deguonies ar sieros grupės, be to, šis žiedas dar gali turėti 1-3 radikalus, kuriais gali būti hidroksilas, halogenas, Cx-C4 alkilas, Cx-C4 - alkoksilas, Cx-C4 - tioalkilas ir Cx-C4 - halogenalkilas;
- 35-naris heteroaromatinis angliavandenilis, turintis 1-3 heteroatomus, kuriais gali būti 2 azoto atomai ir deguonies arba sieros, be to šis žiedas dar gali turėti 1-3 radikalus iš grupių:halogenu, ciano, Cx-C4 - alkilo, Cx-C4 - alkoksilo, Cx-C4 LT 3295 B tioalkilo, C4-C4 - halogenalkilo, C2-C6 - alkenilo, C2-C6 - alkeniloksilo, C2-C6 - halogenalkenilo, C4-C4 - alkoksilo-C1-C4 - alkilo;A 5-membered heteroaromatic hydrocarbon containing 1-3 heteroatoms which may have 2 nitrogen atoms and oxygen or sulfur, and may further contain 1-3 radicals from the group: halogen, cyano, Cx-C4 - alkyl, Cx-C4 - alkoxyl, Cx-C4 LT 3295 B thioalkyl, C4-C4 - haloalkyl, C2-C6 - alkenyl, C2-C6 - alkenyloxyl, C2-C6 - haloalkenyl, C4-C4 - alkoxyl-C1-C4 - alkyl;fenilo arba piridilo grupė, be to Šios grupės gali dar turėti 1-3 radikalus iš grupės: halogenu, nitro, ciano, Cx-C4 - alkilo, C4-C4 - alkoksilo, C4-C4 - tioalkilo, C4-C4 - halogenalkilo, C3-C6 alkeniloksilo, C3-C6 - alkiniloksilo, C4-C4 alkoksilo-C1-C4 - alkilo ir -NRaRb, kur Ra ir Rb turi aukščiau paminėtas reikšmes, o taip pat naudojamos žemės ūkyje jų druskos ir esteriai Ci~C10 - karboninių ir neorganinių rūgščių. phenyl or pyridyl group, the following groups may additionally contain 1-3 radicals from the group: halogen, nitro, cyano, Cx-C4 - alkyl, C4-C4 - alkoxyl, C4-C4 - thioalkyl, C4-C4 - haloalkyl, C3-C6 alkenyloxyl, C3-C6 - alkynyloxyl, C4-C4 alkoxyl-C1-C4 - alkyl and -NRaRb, where Ra and Rb have the meanings given above and their salts and esters Ci ~ C are also used in agriculture10 - carbonic and inorganic acids. 15 2. Herbicidinė priemonė, turinti inertinius priedus ir herbicidiškai veikianti, junginį, besiskirianti tuo, kad herbicidu joje yra cikloheksenonoksimo eteriai bendros I formulės pagal 1 punktą. 15th 2. A herbicide containing an inert additive and a herbicidal compound, characterized in that it contains cyclohexenone oxime ethers of the general formula I according to claim 1.
Independent claims3
2,933 paragraphs in 182 sections, as filed
The present invention relates to novel herbicidally active cyclohexenone oxime ethers having the following formula (I):
R.
<img file="LT3295B_D0001.tif" />
(I) wherein the substituents have the following meanings:
R<sub>1</sub>-C<sub>1</sub>-C<sub>4</sub> - an alkyl group;
AC<sub>2</sub>-C<sub>6</sub> - alkylene or C<sub>3</sub>-C<sub>6</sub> - an alkenylene group, moreover, these groups may have from 1 to 3 C © - © - alkyl groups, halogen atoms;
Z is a 5-membered heteroaromatic hydrocarbon containing from 1 to 3 heteroatoms represented by either 3 nitrogen atoms or oxygen or sulfur; 6-membered heteroaromatic hydrocarbon with 1-4 nitrogen atoms;
X - amino group - NR<sub>a</sub>R<sub>b</sub>, where
R<sub>a</sub> - hydrogen, Cy-C ,, - alkyl group, C<sub>3</sub>-C<sub>6</sub> an alkenyl group or C<sub>3</sub>-C<sub>6</sub> - an alkynyl group and
R<sub>b</sub> - hydrogen, C<sub>r</sub>-C<sub>4</sub> - alkyl group, C<sub>3</sub>-C<sub>6</sub> alkenyl group, C<sub>3</sub>-C<sub>6</sub> - alkynyl group, C, _- C<sub>6 </sub>- an acyl group or a benzoyl radical, in addition to which the aromatic ring may be further substituted with one to three of the following: nitro, cyano, halogen, C<sub>x</sub>-C<sub>4</sub> alkyl, C<sub>x</sub>-C<sub>4</sub> - alkoxyl, {© - (© - thioalkyl and C<sub>1</sub>-C<sub>4</sub> - haloalkyl, nitro, cyano, halo, Ο<sub>χ</sub>-Ο<sub>4</sub> - alkyl, C<sub>1</sub>-C<sub>4</sub> - alkoxyl,
C<sub>x</sub>-C<sub>4</sub> - thioalkyl, C 1 -C 4 - haloalkyl, carboxyl, C<sub>x</sub>-C<sub>4</sub> - haloalkoxyl, alkoxycarbonyl, benzyloxycarbonyl, phenyl, and the aromatic moieties may be further substituted with 1-3 such as: nitro, cyano, halogen, 0-0-alkyl, 0-C<sub>4</sub> - alkoxyl,
0-C<sub>4</sub> - thioalkyl, 0-C<sub>4</sub> - haloalkyl, 0-C<sub>4</sub> haloalkoxyl, carbonyl, 0<sup>-</sup>C<sub>4 </sub>alkoxycarbonyl, benzyloxycarbonyl;
n = 0 to 3 or 1 to 4 in the case Z is a halogen substituted pyridyl radical;
R<sub>2</sub> - 0-0 - alkoxyl-0-0 - alkyl - or 0-0thioalkyl-0-0 - alkyl; C<sub>3</sub>-C<sub>7</sub> - a cycloalkyl group, or C<sub>5</sub>-C<sub>7</sub> - a cycloalkenyl group, in addition these groups may have 1-3 further radicals which may be 0-C<sub>4</sub> - alkyl, 0-C<sub>4</sub> - alkoxyl, 0-0 - thioalkyl, 0-C<sub>4 </sub>- haloalkyl, hydroxy or halogen;
A 5-membered saturated heterocycle containing 12 heteroatoms, such as oxygen or sulfur, and the heterocycle may have 13 more radicals, such as 0-C<sub>4</sub> - alkyl, C<sub>x</sub>-C<sub>4</sub> alkoxyl, 0-0 for thioalkyl and 0-C<sub>4</sub> haloalkyl;
A 6-membered or 7-membered saturated or mono- or double-unsaturated heterocycle containing 1 to 2 heteroatoms as oxygen or sulfur, in addition, this ring may also have 1 to 3 radicals selected from hydroxy, halogen, 0-C<sub>4</sub> - alkyl, 0-0 - alkoxyl, C<sub>x</sub>-C<sub>4</sub> - thioalkyl and 0-C<sub>4</sub> - haloalkyl;
A 5-membered heteroaromatic hydrocarbon containing 13 heteroatoms, such as 2 nitrogen atoms and one oxygen or sulfur atom, and may additionally contain 1-3 radicals from the group: halogen, cyano, 0-C<sub>4</sub> - alkyl, 0<sup>-</sup>C<sub>4</sub> - alkoxyl, C<sub>x</sub>-C<sub>4</sub> - thioalkyl, 0-0 - haloalkyl, C<sub>2</sub>-C<sub>6</sub> - alkenyl, C<sub>2</sub>-C<sub>6</sub> alkenyloxyl, C<sub>2</sub>-C<sub>6</sub> - haloalkenyl and C<sub>x</sub>-C<sub>4</sub>
- alkoxyl-C<sub>1</sub>-C<sub>4</sub> - alkyl;
phenyl group or pyridyl group, in addition, these groups may have 1-3 further radicals from the group: halogen, nitro, cyano, C<sub>x</sub>-C<sub>4</sub> - alkyl, C<sub>x</sub>-C<sub>4</sub> - alkoxyl, C<sub>x</sub>-C<sub>4</sub> thioalkyl, C<sub>x</sub>-C<sub>4</sub> - haloalkyl, C<sub>3</sub>-C<sub>6</sub> - alkenyloxyl, C<sub>3</sub>-C<sub>6</sub> - alkynyloxyl, C<sub>x</sub>-C<sub>4</sub> - alkoxyl-C<sub>1</sub>-C<sub>4</sub>
- alkyl and - NRaRb, Ra and Rb have the meanings given above, as well as their salts and esters C<sub>1</sub>-C<sub>10</sub> - carbonic and inorganic acids.
Further, the invention describes a process for their preparation as well as their use as a plant protection agent.
According to the invention, the cyclohexenones (I) have a pronounced acidic character, that is, they can form simple products of interaction with one another, such as salts of alkali and earth alkaline compounds or enol esters.
The compounds of formula (I) may exist in several tautometric forms, all of which are included within the scope of the invention. Cyclohexenones are described in the literature as herbicides in the general formula (! '),
<img file="LT3295B_D0002.tif" />
wherein, D is benzyl and Ε-2-ethylthiopropyl (U.S. Pat. No. 4,440,566);
D - benzyl, but-2-enyl, and E-substituted 5-membered heteroaryl radical (EP A 238 021, EP A 125 094);
D - benzyl, butenyl-2, and E-substituted phenyl (EP No. A 80 301);
D-but-2-enyl and E-5-7 membered heterocyclic ring having up to two oxygen, sulfur atoms and up to two double bonds (EP A 218 233).
However, there was a need for compounds which, when used in small amounts, exhibit a high degree of selectivity, that is to say they can control undesired plants without damaging the crop.
In accordance with this task, novel cyclohexenone oxime ethers of formula I have been obtained which have good herbicidal activity in combating unwanted herbs. The compounds do not harm crop plants as well as some bell crops, such as rice.
The cyclohexenones of Formula I can be obtained by known methods from the known compounds of Formula II A 125 094, EP-A-0404. AA 137 174 and EP no. hydroxylamine (EP No. A 80,301, EP No. A 4,249,937, EP No. 10 / 1S.1181 ff and corresponding formulas III).
(EP No A 169 521) derivatives 142 741,
A 177 913) (Houben-Weyl,
<img file="LT3295B_D0003.tif" />
<img file="LT3295B_D0004.tif" />
X
It is expedient for these compounds to interact in a heterogeneous phase in a solvent at temperatures below 80 ° C in the presence of bases and using hydroxylamine (III) ammonium salts.
Bases which may be used are, for example, carbonates, bicarbonates, acetates, alcoholates or alkali and earth alkaline metal oxides, in particular sodium, potassium hydroxides, magnesium, calcium oxides. In addition, organic bases such as pyridine or tertiary amines may be used. The bases are introduced, for example, from 0.5 to 2 m-equiv., Based on the ammonium compound.
Suitable solvents are, for example, dimethylsulfoxide; alcohols: methanol, ethanol and isopropanol; aromatic hydrocarbons benzene and toluene; chlorinated hydrocarbons: chloroform and dichloroethane; aliphatic hydrocarbons; hexone and cyclohexane; esters such as ethyl acetate and ethers such as diethyl ether, dioxane, tetrahydrofuran. The reaction is carried out in methanol in the presence of sodium bicarbonate.
The reaction ends in a few hours. The target compound can be isolated, for example, by concentration of the mixture, separation of the residue in the methylene chloride / water mixture and distillation of the solvent under reduced pressure.
The reaction may be carried out immediately using the free hydroxylamine base, for example in aqueous solution; depending on the solvent used for the compounds II, the reaction mixture may be single or biphasic.
the following solvents may be suitable for this embodiment: alcohols such as methanol, ethanol, isopropanol and cyclohexanol; aliphatic and aromatic hydrocarbons as well as chlorine-containing hydrocarbons such as hexane, cyclohexane, methylene chloride, toluene, dichloroethane; esters such as ethyl acetate; nitriles such as acetonitrile; and cyclic ethers such as dioxane and tetrahydrofuran.
The alkali metal salts of the compounds may be prepared by treating the 3-hydroxy compounds with sodium or potassium hydroxide or alcoholate in aqueous solution or in an organic solvent such as methanol, ethanol, acetone or toluene.
Other metal salts such as manganese, copper, zinc, 5 iron; calcium, magnesium and barium may be obtained from sodium salts by conventional means, as well as ammonium and phosphonium salts with ammonia, phosphonium, sulfonium or sulfoxonium hydroxide.
Type II compounds may be prepared by conventional methods (Tetrahedron Lett., 2491 (1975)), for example from the corresponding cyclohexane-1,3-dione Formula IV.
<img file="LT3295B_D0005.tif" />
wherein Y is hydrogen or methoxycarbonyl
Compounds of formula II may also be obtained via the intermediate enol ester intermediates which are prepared by interaction of compounds of formula IV with acid chloro anhydrides in the presence of bases and subsequent conversion with imidazole or pyridine derivatives (JP-OS
79/063 052).
<img file="LT3295B_D0006.tif" />
The compounds of formula IV are obtained in a number of known process steps on the basis of known, previously obtained products.
The synthesis of hydroxylamine (III) wherein A is an unsubstituted but-3-enylene bridge is carried out according to the reaction scheme below;
HD-AZX<sub>n</sub>
VII γ- / | -Ζ ~ Χη
Fruit
II
Vin +
II
V
VI +>
<img file="LT3295B_D0007.tif" />
-Ο-Α-2-Χη
Vi ί> IH
Y is a leaving group such as halogen-chlorine, bromine and iodine or CH<sub>3</sub>SO<sub>2</sub> - Oh
Alkylating agents (VIII) can be prepared by known methods [cf.: '' Cyclopropylhetaryl - Carbinols rearrangement. J. Heterocycl. Chem. 14, 525 (1976), JP 55 051 004, JP 55 047 601; Houben-Weyl: Methods in Organic Chemistry, vol. 4/3, p. 424 et al. p .: Combination of metal-containing heterocycles with 1, ω-dibromoalkanes: DE-A 28 21 409 and Chem. Ber. 114, 3667 (1981)].
Alkylating agents can be obtained from carbinols (VII) by a known method. [Combination of hetaryl iodides, bromides with 1, ω-alkenols in the presence of palladium catalysts: Tetrahedron 35, 329 (1979); Chem. Lett., 423 (1977); Houben-Weyl; Organic Chemistry Methods Vol. 5/3, p. 862 et seq. 899 et seq., Vol. 5/4, p. 361 et seq.]. In particular, the alkylating agent is coupled with the cyclic hydroxyimide (V) and cleaves the resulting hydroxylamine derivative (VI) to the free hydroxylamine (III) with 2-aminoethanol.
In cyclic hydroxyimides (V), D is, for example, C<sub>2</sub>-C<sub>3</sub> - alkylene, C<sub>2</sub> - alkenylene or a 5- or 6-membered ring having 1-3 double bonds and 1 nitrogen atom, for example, phenylene, pyridinylene, cyclopentylene, cyclohexylene, for example the following or cyclohexene compounds:
len. This is,
<img file="LT3295B_D0008.tif" />
<img file="LT3295B_D0009.tif" />
<img file="LT3295B_D0010.tif" />
Interaction of compounds VIII with hydroxyimides V is conveniently carried out in the presence of bases. Any base capable of deprotonating hydroxyimides V without touching the imid system is suitable. These are so-called non-nucleophilic bases. Mineral bases such as alkali and earth alkaline carbonates and bicarbonates may be mentioned; organic bases such as aliphatic, cycloaliphatic and aromatic tertiary amines. A mixture of these bases may also be used.
As examples of individual compounds, the following bases may be mentioned: sodium, potassium, magnesium, calcium, barium carbonates and bicarbonates, trimethylamine, triethylamine, tributylamine, ethyldiisopropylamine, N, N-dimethylaniline, 4-N, N-dimethylaminopyridine, diazobicyclooctane, -methylpiperidine, 1,4-dimethylpiperazine, pyridine, quinoline, bipyridine, phenanthroline. Preference is given to the cheapest bases: sodium and potassium carbonates.
The bases are usually added in equivalent amounts or may be present in excess of up to 5 equivalents, converted to hydroxyimide. Larger surpluses are possible, but not an added priority. Minor amounts of bases may also be used. However, the amount of bases usually added is
1-3, preferably 1-2 equivalents, expressed as hydroxyimide.
It is possible to use, for example, hydroxides, in this case also nucleophilic bases, such as alkali and alkaline earth metals, in particular sodium and potassium hydroxides. it is preferred that the bases are introduced in equivalent amounts relative to hydroxyimide (V) to prevent nucleophilic attack on the carbonyl group of the imide system by hydroxyl ions.
It is expedient to carry out the reaction of the starting compounds (VIII) with hydroxyimides (V) in a solvent to help maintain certain reaction conditions. Suitable solvents are, for example, polar-aprotic solvents such as dimethylformamide, N-methylpyrrolidone, dimethylsulfoxide, sulfolane and cyclic ureas. The amount of solvent in general does not play a special role.
Interaction of the starting compounds (VIII) with hydroxyimides (V) can also occur via transition phase catalysis.
In this case, a solvent consisting of two phases with water is used. Suitable quaternary ammonium and phosphonium salts, polyethylene glycols, polyethylene glycol ethers and Kraun ethers as described in Dehmlow et al., Phase Transfer Catalysis, p. 37-45 and 86-93, Verlag Chemie, Weinheim 1980. It is expedient to use from 1 to 10% v / v, preferably from 3 to 5% v / v, of the transition phase catalysts based on the total volume of the reaction mixture.
The reaction of the starting compounds (VIII) with hydroxyimides (V) takes place at temperatures between 0 and 140 ° C, preferably between 20 and 100 ° C, more preferably between 40 and 80 ° C. In addition, it is important that the hydroxyimide (V) together with the bases is added to the solvent and the starting product (VIII) is dosed into this solution. Advantageously, the hydroxyimide is introduced at a reduced temperature, for example 0-50 ° C, after which the reaction mixture is heated to the temperature necessary for the reaction.
At the end of the reaction, the cooled reaction mixture is stirred with water while the resulting hydroxylamine derivatives (VI) are separated in the form of a crystalline solid or an oil. The hydroxylamine derivatives thus obtained can be further purified by recrystallization or extraction.
Hydroxylamine derivatives (VI) may be isolated as intermediates or immediately converted to hydroxylamine (III) with the free amino group. This reaction can be carried out in known manner as described, for example, in DE no. A 36 15 973 in the publications cited above. The method according to DE no. A 36 15 973 wherein the hydroxylamine derivatives (III) are isolated by ethanolamine. It is also possible to isolate the hydroxylamine derivatives (III) with other bases such as aqueous mineral base solutions, amines, hydrazines, hydroxylamines or aqueous acid solutions.
From the reaction mixtures obtained by these methods, the hydroxylamine derivatives (III) can be isolated by conventional methods, for example, by extraction or crystallization. The tendency of these hydroxylamine derivatives to increase crystallization may be to be converted into salts with the aid of mineral and organic acids. To this end, dilute solutions of these acids react with hydroxylamine derivatives in addition to amounts. The resulting hydroxylamine hydroxylamine with the free amino group can be further processed directly into equivalent salt salts, as derivatives, into Form I herbicides or stored as such.
Including biological activity, preference is given to cyclohexenones of formula I where the substituents have the following meanings:
R<sub>x</sub> alkyl, such as methyl, ethyl, propyl, 1-methylethyl, butyl, 1-methylpropyl, 2-methylpropyl, 1,1-dimethylethyl, pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 1,1-dimethylpropyl, 1,2 -dimethylpropyl, 2,2-dimethylpropyl, 1-ethylpropyl, hexyl, 1-methylpentyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 1,1-dimethylbutyl, 1,2-dimethylbutyl, 1,3-dimethylbutyl, 2 , 2-dimethylbutyl, 2,3-dimethylbutyl, 3,3-dimethylbutyl, 1-ethylbutyl,
2-ethylbutyl, 1,1,2-trimethylpropyl, 1,2,2-trimethylpropyl, 1-ethyl-1-methylpropyl and 1-ethyl-2-methylpropyl, especially ethyl and propyl.
A - alkylene or alkenylene such as ethylene, propylene, propenylene-2, butylene, butenylene-2, butenylene-3, pentylene, pentenylene4, hexylene, hexenylene-5, and the above groups may be substituted one or three times with methyl or ethyl and / or fluorine or chlorine; both unsaturated chains may be present in both the eis and the trans. Particularly suitable are butenylene-2 and butenylene-3;
Z - 5-membered heteroaryl such as furanyl, pyrrolyl, thienyl, imidazolyl, pyrazolyl, isoxazolyl, oxazolyl, isothiazolyl, thiazolyl, oxadiazolyl, thiadiazolyl, triazolyl, especially furanyl and thionyl, 6-membered heteroaryl, e.g. , pyrazil, triazyl, tetrazyl, especially pyridyl and pyrimidyl;
X is nitro, cyano, halogen such as fluorine, chlorine, bromine and iodine, especially fluorine and chlorine; alkyl such as methyl, ethyl, propyl, 1-methylethyl, butyl, 1-methylpropyl, 2-methylpropyl and 1,1-dimethylethyl, especially methyl and 1,1-dimethylethyl, alkoxyl such as methoxyl, ethoxyl, propoxyl, 1 -methylethoxy, butoxyl, 1-methylpropoxyl, 2-methylpropoxyl and 1,1-dimethylethoxy, especially ethoxyl, 1-methylethoxy and 1,1-dimethylethoxy, thioalkyl such as thiomethyl, thioethyl, thiopropyl, 1-thiomethylethyl, thiobutyl, 1thiomethylpropyl, 2-thiomethylpropyl and 1,1-thiodimethylethyl, especially thiomethyl and thioethyl, haloalkyl, for example methyl, trifluoromethyl, dichlorofluoromethyl, fluoromethyl, difluorochlorodifluoromethyl, 1-fluorotrichloromethyl ethyl, 2-fluoroethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl. chloro-2, 2-difluoroethyl, 2,2-dichloro-2-fluoroethyl, 2,2,2-trichloroethyl and pentafluoroethyl, especially difluoromethyl, trifluoromethyl, 2,2,2-trifluoroethyl and pentefluoroethyl, haloalkoxy, e.g. difluoromethoxyl, trifluoromethoxyl, chlorodifluoromethoxyl, dichlorofluoromethoxyl, 1-fluoroethoxyl, 2-fluoroethoxyl, 2,2-difluoroethoxyl, 1,1,2,2-tetrafluoroethoxyl, 2-chloro-1,2,3-trifluoroethoxyl, pentafluoroethoxyl, especially trifluoroethyl , alkoxycarbonyl such as methoxycarbonyl, ethoxycarbonyl, propyloxycarbonyl, 1-methylethoxycarbonyl, butoxycarbonyl and 1,1<sup></sup>dimethylethoxycarbonyl, especially methoxycarbonyl, ethoxycarbonyl and 1,1-dimethylethoxycarbonyl, preferably methoxycarbonyl.
carbonyl, referred to
Benzyloxycarbonyl and phenyl, in addition, the aromatic moieties may in turn contain from 1 to 3 such moieties: nitro, cyano, carboxyl, benzyloxyhalogen as defined in X; alkyl, R<sub>x</sub>especially methyl, ethyl, 1-methylethyl, alkoxyl as above, ethoxyl; especially above, thioalkyl, thiomethyl; particularly particularly methoxyl and, as above, haloalkyl is trifluoromethyl; haloalkoxyl as above, in particular difluoromethoxyl and trifluoromethoxyl and / or alkoxycarbonyl as above, especially methoxycarbonyl and ethoxycarbonyl.
Amine group - NR<sub>a</sub>R<sub>b</sub>:
R<sub>a</sub> - hydrogen;
alkyl, for example methyl, ethyl, propyl, 1-methylethyl, butyl, 1-methylpropyl, 2-methylpropyl and 1,1-dimethylethyl, especially methyl and ethyl;
propenyl, propenyl, alkenyl such as 2-propenyl, 2-butenyl,
3-butenyl, 1-methyl-2-propenyl, 2-methyl-2-propenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl,
1-methyl-2-butenyl, 2-methyl-2-butenyl, 3-methyl-2-butenyl, 1-methyl-3-butenyl, 2-methyl-3-butenyl, 3-methyl-3-butenyl, 1,3-dimethyl- 21,2-dimethyl-2-propenyl, 1-ethyl-22-hexenyl, 3-hexenyl, 4-hexenyl, 5-hexenyl, 1-methyl-2-pentenyl, 2-methyl-2-pentenyl, 3-methyl-2-pentenyl, 4-methyl-2-pentenyl, 1-methyl-3-pentenyl, 2-methyl-3-pentenyl, 3-methyl-3-pentenyl, 4-methyl-3-pentenyl, 1-methyl-4-pentenyl, 2-methyl- 4-pentenyl,
3-methyl-4-pentenyl, 4-methyl-4-pentenyl, 1,1-dimethyl-2-butenyl, 1,1-dimethyl-3-butenyl, 1,2-dimethyl-2-butenyl, 1,2-dimethyl-3- butenyl, 1,3-dimethyl-2-butenyl, 1,3-dimethyl-3-butenyl, 2,2-dimethyl-3-butenyl, 2,3-dimethyl-2-butenyl, 1-ethyl-2-butenyl, 1-ethyl-3- butenyl, 2-ethyl-2-butenyl, 2-ethyl-3-butenyl, 1,1,2-trimethyl-2-propenyl, 1-ethyl-1-methyl-2-propenyl and 1-ethyl-2-methyl-2-propenyl, especially 2 -propenyl and 2-butenyl;
Rb is hydrogen;
allyl as above;
alkenyl as above;
alkynyl such as 2-propynyl, 2-butynyl,
2-pentynyl, 3-pentynyl, 4-pentynyl, 1-methol-3-butynyl, 2-methyl-3-butynyl, 1-methyl-2-butynyl, 1,1-dimethyl-2-propynyl, 1-ethyl-2- propinyl, 2-hexinyl, 3-hexinyl, 4-hexinyl,
5-hexinyl, 1-methyl-2-pentynyl, 1-methyl-3-pentynyl, 1-methyl-4-pentynyl, 2-methyl-3-pentynyl, 2-methyl-4-pentynyl, 3-methyl-4- pentinyl,
4-methyl-2-pentynyl-, 1,1-dimethyl-2-butynyl,
1,1-dimethyl-3-butynyl, 1,2-dimethyl-3-butynyl,
2,2-dimethyl-3-butynyl, 1-ethyl-2-butynyl, 1-ethyl-3-butynyl, 2-ethyl-3-butynyl and 1-ethyl-methyl-2-propynyl, especially 2-propynyl and 2-butynyl;
acyl groups such as acetyl, propionyl, butyryl, 2-methyl-propionyl, pentanoyl, 2-methylbutyryl, 3-methyl-butyryl, 2,2-dimethylpropionyl, hexanoyl, 2-methylpentanoyl, 3-methylpentanoyl, 4-methylpentanoyl, 2,2-dimethylbutyryl , 2,3-dimethylbutyryl, 3,3-dimethylbutyryl and 2-ethylbutyryl, in particular acetic acid and propionyl or benzoyl radical, in addition the aromatic radical may have from 1 to 3 such radicals: nitro, cyano, carboxyl, benzyloxycarbonyl, halogen as defined for X;
alkyl as defined for R<sub>x</sub>especially methyl, ethyl and 1-methylethyl;
alkoxyl as above, in particular methoxyl and ethoxyl;
thioalkyl as above, especially thiomethyl;
haloalkyl as defined above, especially trifluoromethyl;
haloalkoxyl as defined above, in particular difluoromethoxy and trifluoromethoxy and / or alkoxycarbonyl and ethoxycarbonyl;
n = 0, -1, 2 or 3, in particular 0, 1 and 2, in the case where the Z-halogen is substituted with a prairidyl radical, then n = 1-4. Preferably n = 0, 1 or 2. The X substituents of some residues may be the same or different;
R<sub>2</sub> alkyl as defined in X, as well as pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl, 2,2-dimethylpropyl, 1-ethylpropyl, hexyl, 1-methylpentyl, 2- methylpentyl, 3-methylpentyl, 4-methylpentyl, 1,1-dimethylbutyl, 1,2-dimethylbutyl, 1,3-dimethylbutyl, 2,2-dimethylbutyl,
2,3-dimethylbutyl, 3,3-dimethylbutyl, 1-ethylbutyl, 1,1,2-trimethylpropyl, 1,2,2-trimethylpropyl, 1-ethyl-1-methylpropyl and 1-ethyl-2-methylpropyl, which may be substituted by alkoxyl or thioalkyl groups represented by X, preferably 1-, 2- or 3-positions, in particular 2-thioethylpropyl;
5-membered heterocycloalkyl, e.g.<sub>1</sub>-C<sub>4</sub> - alkoxyl groups, C<sub>1</sub>-C<sub>4</sub> - thioalkyl groups and / or C<sub>x</sub>-C<sub>4</sub> haloalkyl groups,
5-membered heteroaryl such as pyrrolyl, pyrazolyl, imidazolyl, isoxazolyl, oxazolyl, isothiazolyl, thiazolyl, furanyl and thienyl, especially isoxazolyl and furanyl,
A 6- or 7-membered heterocycle, such as tetrahydropyranyl-3, dihydropyranyl-3, tetrahydropyranyl-4, dihydropyranyl-4, tetrahydrothiopyranyl-3, dihydrothiopyranyl-4, dihydrothiopyranyl-4, and dihydropyranyl-5, especially tetrahydropyranyl-5, , tetrahydropyranyl-4 and tetrahydrothiopyranyl-3, phenyl or pyridyl radical, in addition the cyclic radical may have 1-3 alkyl groups, alkoxyl groups, thioxyl groups and / or haloalkyl groups.
5-membered heteroaromatic hydrocarbons R<sub>2</sub> may be substituted by the following radicals:
a halogen atom as defined for X, especially fluorine and chlorine, alkoxyalkyl such as methoxymethyl, 2-methoxyethyl, 2-methoxypropyl, 3-methoxypropyl, 2-methoxy-1-methylethyl, ethoxymethyl, 2-ethoxyethyl, 2-ethoxypropyl, 3-ethoxypropyl, 2-ethoxy-1-methylethyl and 1-ethoxy-1-methylethyl, especially methoxyethyl and ethoxyethyl, alkenyl such as ethenyl, 1-propenyl, 2-propenyl, 1-methylethenyl, 1-butenyl, 2-butenyl, 3-butenyl, 1 -methyl-1-propenyl, 1-methyl-2-propenyl, 2-methyl-1-propenyl, 2-methyl-2-propenyl, 1-pentenyl, 2-pentenyl, 3pentenyl, 4-pentenyl, 1-methyl-1-butenyl, 2-methyl-butenyl, 3-methyl- l-butenyl, l-methyl-2-butenyl, 2-methyl-2-butenyl,
3-methyl-2-butylene 3295 B butenyl, butenyl, butenyl, nyl, 1-methyl-3-butenyl, 2-methyl-3-butenyl,
3-methyl-3-butenyl, 1,1-dimethyl-2-propenyl,
1,2-dimethyl-1-propenyl, 1,2-dimethyl-2-propenyl, 1-ethyl-1-propenyl, 1-ethyl-2-propenyl, 1hexenyl, 2-hexenyl, 3-hexenyl, 4hexenyl, 5- hexenyl, 1-methyl-1-pentenyl, 2-methyl-1-pentenyl, 3-methyl-1-pentenyl, 4-methyl-1-penentenyl, 1-methyl-2-pentenyl, 2-methyl-2-pentenyl, 3- methyl 2-pentenyl, 4-methyl-2-pentenyl, 1-methyl-3-pentenyl, 2-methyl-3-pentenyl,
3-methyl-3-pentenyl, 4-methyl-3-pentenyl, 1-methyl-4-pentenyl, 2-methyl-4-pentenyl, 3-methyl-4-pentenyl, 4-methyl-4-pentenyl, 1,1-dimethyl- 2-butenyl, 1,1-dimethyl-3-butenyl, 1,2-dimethyl-1,2-dimethyl-2-butenyl, 1,2-dimethyl-31.3-dimethyl-1-butenyl, 1,3-dimethyl-21.3- dimethyl-3-butenyl, 2,2-dimethyl-3-butenyl, 2,3-dimethyl-1-butenyl, 2,3-dimethyl-2-butenyl, 2,3-dimethyl-3-butenyl, 3,3-dimethyl-1-butenyl, 1-ethyl-1-butenyl, 1-ethyl-2-butenyl, 1-ethyl-3-butenyl, 2-ethyl-1-butenyl, 2-ethyl-2-butenyl, 2-ethyl-3-butenyl, 1,1,2-trimethyl-2-propenyl, 1-ethyl-1-methyl-2-propenyl, 1-ethyl-2-methyl-1-propenyl, and 1-ethyl -2-methyl-2-propenyl, in particular 1-methylethenyl or the corresponding alkenyloxy and / or haloalkenyl.
6- and 7-membered heterocycles may have hydroxyl groups in addition to the substituents listed above.
The phenyl and pyridyl radicals may be substituted in addition to the above, including the following radicals:
alkenyloxyl such as 2-propenyloxyl, 2-butenyloxyl, 3-butenyloxyl, 1-methyl-2-propenyloxyl, 2-methyl-2-propenyloxyl, 2LT 3295B pentoxyl, 3-pentenyloxyl, 4-pentenyloxy, 1-methyl-2-butenyloxyl , 2-methyl-2-butenyloxyl, 3-methyl-2-butenyloxyl, 1-methyl-3-butenyloxyl, 2-methyl-3-butenyloxyl, 3-methyl-3-butenyloxyl, 1,1-dimethyl-2-propenyloxy, , 2-dimethyl-2-propenyloxyl, 1-ethyl-2-propenyloxyl, 2-hexenyloxyl, 3-hexenyloxyl, 4hexenyloxyl, 5-hexenyloxyl, 1-methyl-2-pentenyloxy, 2-methyl-2-pentenyloxy, 3-methyl-2-pentenyloxy, 4-methyl-2-pentenyloxy, 1-methyl-3-pentenyloxy, 2-methyl-3-pentenyloxy, 3- methyl-3-pentenyloxy, 4-methyl-3-pentenyloxy, 1-methyl-4-pentenyloxy, 2-methyl-4-pentenyloxy, 3-methyl-4-pentenyloxy, 4-methyl-4-pentenyloxy, 1,1-dimethyl-2-butenyloxyl, 1,1-dimethyl-3-butenyloxyl, 1,2-dimethyl-2-butenyloxyl, 1,2-dimethyl-3-butenyloxyl, 1,3-dimethyl-2-butenyloxyl, 1,3-dimethyl-3-butenyloxyl, 2,2-dimethyl-3-butenyloxyl, 2,3-dimethyl-2-butenyloxyl, 2,3-dimethyl-3-butenyloxyl, 1-ethyl-2-butenyloxyl,
1-ethyl-3-butenyloxyl, 2-ethyl-2-butenyloxyl,
2-ethyl-3-butenyloxyl, 1,1,2-trimethyl-2-propenyloxyl, 1-ethyl-1-methyl-2-propenyloxy and 1-ethyl-2-methyl-2-propenyloxy, in particular 2-propenyloxy and 2-butenyloxyl;
alkynyloxyl such as 2-propynyloxyl, 2-butynyloxyl, 3-butynyloxyl, 1-methyl-2-propynyloxy, 2-pentyloxy, 3-pentyloxy, 4-pentyloxy, 1-methyl-3-butynyloxyl, 2-methyl-3-butynyloxy, 1- methyl 2-butynyloxyl, 1,1-dimethyl-2-propynyloxyl, 1-ethyl-2-propynyloxyl, 2-hexynyloxyl, 3-hexynyloxyl, 4-hexynyloxyl, 5-hexynyloxyl, 1-methyl-2-pentynyloxyl, 1-methyl-3- pentynyloxyl, 1-methyl-4-pentynyloxyl, 2-methyl-3-pentynyloxy LT 3295 B glass, 2-methyl-4-pentynyloxy, 3-methyl-4-pentyloxy, 4-methyl-2-pentyloxy, 1,1-dimethyl-2-butynyloxyl, 1,1-dimethyl-3-butynyloxyl, 1,2-dimethyl-3-butynyloxyl, 2,2-dimethyl-3-butynyloxyl, 1-ethyl-2-butynyloxyl, 1-ethyl-3-butynyloxyl, 2-ethyl-3-butynyloxyl and 1-ethyl-1-methyl-2-propynyloxyl, especially 2-propynyloxyl and 2-butynyloxyl ;
alkoxyalkyl as above;
-NR<sub>a</sub>R<sub>b</sub>, as in X.i.
R<sub>lf</sub> R<sub>2</sub>, and the W radicals are introduced in a similar manner into the D and E (W = Z - Xn) ethers of cyclohexenone oxime,
<img file="LT3295B_D0011.tif" />
-0CH<sub>2</sub>-CH = CH 'CH<sub>2</sub><sub>R</sub>.
<img file="LT3295B_D0012.tif" />
In this case, the corresponding hydroxylamines (III) are preferred. Cyclohexenone oxime ethers (I) are used as herbicides, in particular to combat plants of the grass family.
Cyclohexenone oxime ethers (I) or herbicidal preparations based thereon may be used directly for spraying, dispersing, dispersing or dispersing powders, suspensions as well as dispersions, granules in high concentration in aqueous, oily or other suspensions, emulsions, oily pastes, by spraying, dispersing or watering. The forms of use depend on the purpose; in each case, a uniform distribution of the biologically active substance must be guaranteed in accordance with the invention.
Compounds (I) are suitable for the manufacture of solutions for direct spraying of emulsions, pastes or oily dispersions. Inert additives may include medium to high boiling mineral oils, such as kerosene or diesel oil, as well as coal tars, oils as well as oils of plant or animal origin, cyclic, aliphatic and aromatic hydrocarbons, e.g. toluene, xylene, paraffin, tetrahydronaphthalene, alkylated naphthalenes or their derivatives, methanol, ethanol, propanol, butanol, cyclohexanol, cyclohexanone, chlorobenzene, isophorone or strongly polar solvents such as NN-dimethylformamide, dimethylsulfoxide, N-methylpyrrolidone or water.
Aqueous use forms can be prepared from emulsion concentrates, dispersions, pastes, binders or water dispersible granules by the addition of water. For the preparation of emulsions, pastes or oily dispersions, they may be used immediately or dissolved in an oil or solvent and homogenized in water with the aid of a humectant, binder, dispersant or emulsifier. Also, concentrates suitable for dilution with water may be obtained from the active ingredient, wetting agent, binder, dispersant or emulsifier, and possibly solvent or oil.
Surfactants may include alkali salts, alkaline earth metals and ammonium salts, aromatic sulfonic acids such as lignin, phenol, naphthalene and dibutylnaphthalenesulfonic acid, as well as alkyl and laarylethyl and fatty acids of fatty acids. sulphates of alcohols as well as salts of glycated ethers of sulphated hexa-, hepta- and octadecanols as well as of fatty alcohols, condensation products of sulfurized naphthalic and naphthalenesulphonic acids with phenol and formaldehyde, polyoxyethylene octylphenol ethers, ethoxylated isooctyl, octyl or nonyl phenol, alkylphenol, tributylphenylpolyglycolate ethers, alkylarylpolypolyethyl alcohol, isotridecyl alcohol, polyglycol ethers of lauryl alcohol, sorbitol esters, solutions obtained from lignin sulphite or methyl cellulose.
Powder dispersible and sprayable materials may be prepared by mixing or co-rinsing biologically active agents with solid excipients.
Granules, for example, in shell, soaked and homogenized, can be made by crushing biologically active substances on solid fillers. Solid aggregates include mineral earths such as silica, silica gel, silicates, talc, kaolin, lime, limestone, chalk, bolus, lye, clay, dolomite, diatomaceous earth. Ca and Mg sulphates, magnesium oxide, ground plastics, fertilizers such as ammonium sulphate, phosphate or nitrate, urea and plant products such as cereal flour, tree bark, tree and nut shells, cellulose powder and other solid fillers.
The prepared forms contain from 0.02 to 95% by weight, preferably from 0.5 to 90% by weight. biologically active substances. In addition, biologically active substances having a purity of from 90 to 100%, preferably from 95 to 100% (by NMR spectrum) are used.
The herbicidal agents (I) according to the invention may be formulated, for example, in the following forms:
1. Mix 90 lbs. d. No. Of compound 8.01 with 10 wt. d. N-methyl-α-pyrrolidone and obtain a solution suitable for use in the form of the smallest droplets.
2. 20 lbs d. No. Compound 8.02 is dissolved in a mixture of 80% by weight. d. of xylene, 10 wt. d. of the product obtained when 8-10 mol of ethylene oxide is added to 1 mol of oleic acid N-monoethanolamide, 5% by weight. d. calcium salts of dodecylbenzenesulfonic acid and 5% by weight. d. of the product obtained by the addition of 40 moles of ethylene oxide to 1 mol of castor oil. Due to spillage and uniform distribution of solution, 100,000 lbs. d. an aqueous dispersion containing 0.02% w / w is obtained in water. biologically active substances.
3. 20 lbs d. No. Compound 8.03 is dissolved in a mixture of 40% by weight. d. of cyclohexanone, 30 wt. d. isobutanol 20 l. d. of the product obtained when 7 moles of ethylene oxide and 10% by weight are added to 1 mole of isooctylphenol. d. of the product obtained by the addition of 40 moles of ethylene oxide to 1 mol of castor oil. Thanks to the spill and the good distribution of the solution, 100,000 lbs. d. an aqueous dispersion containing 0.02% w / w is obtained in water. biologically active substances.
LT 3291 B
4. 20 lbs d. biologically active substance no. 8.04 is dissolved in a mixture of 25% by weight. d. of cyclohexanone, 65 lbs. d. fractions of a mineral oil boiling in the range of 210 to 280 ° C and 10% by weight; d. of the product obtained by the addition of 40 moles of ethylene oxide to 1 mol of castor oil. Thanks to the spill and distribution of the solution, 100,000 lbs. d. an aqueous dispersion containing 0.02% w / w is obtained in water. biologically active substances.
5. 20 lbs d. biologically active substance no. 8.05 mix well with 3 wt. d. sodium salt of diisobutylnaphthalene-a-sulfonic acid, 17% by weight. d. sodium salt of lignin sulphonic acid, worked from sulphite alkali and 60% by weight; d. powdered silica gel and ground in a pulverizing mill. Thanks to the gentle distribution of the mixture at 20,000 sv d. water spray solution containing 0.1% w / w biologically active substances.
6th 3 lbs d. biologically active substance no. 8.06 mixed with 97 lbs. d. finely dispersed kaolin. In this way, a spray containing 0.1% wt. biologically active substances.
7th 30 lbs d. biologically active substance no. 8.07 mix well with 92 lbs. d. powdered silica gel and 8 wt. d. paraffin oil, which is sprayed onto the surface of this silica gel. In this way, a ready-form form of the biologically active substance with good adhesive properties is obtained.
8th 20 lbs d. biologically active substance no. 8.08 mix well with 2 lbs. d. calcium salts of dodecylbenzenesulfonic acid, 8% by weight. d.
polyglycol ether of fatty alcohols, 2 wt. d. phenol-urea-formaldehyde-condensate sodium, and 68 IU. d. of mineral paraffin oil. A stable oily dispersion is obtained.
These tools can be used either before or after sprouting. If any crop is susceptible to biologically active substances, a technique such as spray application of the herbicide may be used in such a way that the leaves of the susceptible crop are not damaged as far as possible and the leaves of exposed plants or open soil are treated with biologically active substances -directed, lay-by).
During the season when germinating target plants are treated, the use of biologically active substances is 0.001-3 kg / ha, preferably 0.01-2 kg / ha. In addition to the inventive range of action against weeds, the sensitivity of crop plants and their desirable effects on growth, as well as the versatility of the methods used, the compounds of the invention can be used for many crop plants. Examples of such cultures include:
LIST OF PLANTS
Botanical name Lithuanian name
Allium cepa
Pineapple comosus
Arachis hypogaea
Asparagus officinalis
Avena sativa
Beta vulgaris spp. altissima turnip onion pineapple peanuts asparagus oats sugar beets
Botanical name Lithuanian name
Beta vulgaris spp. rapa fodder beet
<td>Beta vulgaris spp. esculenta</td><td>Red beet</td>
<td>Brassica napus var. napus</td><td>rape</td>
<td>Brassica napus var. napobrassica</td><td>harshness, satanic</td>
<td>Brassica napus var. rapa</td><td>white beets</td>
<td>Brassica rapa var. silvester</td><td>radish</td>
<td>Camellia sinensis</td><td>tea</td>
<td>Carthamus tinctorius</td><td>dyed safflower</td>
<td>Carya illinoinensis</td><td>pecan nut</td>
<td>Citrus limon</td><td>lemon</td>
<td>Citrus maxima</td><td>pampelmus</td>
<td>Citrus reticulata</td><td>mandarin</td>
<td>Citrus sinensis</td><td>Orange</td>
<td>Coffea arabica (Coffea canephora,</td><td></td>
<td>Coffea liberica)</td><td>coffee tree</td>
<td>Cucumis is lying</td><td>cucumber</td>
<td>Cucumis sativus</td><td>cucumbers</td>
<td>Cynodon dactylon</td><td>noodle</td>
<td>Daucus carota</td><td>carrots</td>
<td>Elaeis guineensis</td><td>oil palm</td>
<td>Fragaria vesca</td><td>strawberry</td>
<td>Clycic max</td><td>soybeans</td>
Gossypiun hirsutum (Gossypiun arboreun,
<td>Gossypiu berbaccun, Gossypiu vitifolium)</td><td>cotton</td>
<td>Helianthus annuus</td><td>sunflower</td>
<td>Helianthus tuberosus</td><td>Jerusalem artichoke</td>
<td>Botanical name</td><td>Lithuanian name</td>
<td>Hevea brasiliensis</td><td>rubber</td>
<td>Hordeum vulgare</td><td>barley</td>
<td>Humulus lupulus</td><td>hops</td>
<td>Ipomoea batat</td><td>sweet potato</td>
<td>Juglans regia</td><td>walnut</td>
<td>Lactuca sativa</td><td>head lettuce</td>
<td>Lens culinaris</td><td>lens</td>
<td>Linum usitatissimum</td><td>linen</td>
<td>Lycopersicon lycopersicum</td><td>tomatoes</td>
<td>Malus spp.</td><td>Apple tree</td>
<td>Manihot esculenta</td><td>cassava</td>
<td>Medicago sativa</td><td>alfalfa</td>
<td>Mentha piperita</td><td>pepper</td>
<td>Fly ssp.</td><td>banana</td>
<td>Nicotiana tabacum (N. rustica)</td><td>tobacco</td>
<td>Olea europaea</td><td>olive tree</td>
<td>Oryza sativa</td><td>rice</td>
<td>Panicum miliaceum</td><td>cannabis</td>
<td>Phaseolus lunatus</td><td>beans</td>
<td>Phaseolus mungo</td><td>arachis</td>
<td>Phaseolus vulgaris</td><td>beans dwarf shrubs</td>
<td>Pennisetum glaucum</td><td>Italian sherry</td>
Petroselinum crispum spp. tuberosum parsley
Picea abies
Abies alba spruce larch
<td>Botanical name</td><td>Lithuanian name</td>
<td>Pinus spp.</td><td>pine tree</td>
<td>Pisum sativum</td><td>vegetable peas</td>
<td>Prunus avium</td><td>cherry</td>
<td>Prunus domestica</td><td>plum</td>
<td>Prunus dulcis</td><td>almonds</td>
<td>Prunus persica</td><td>peach</td>
<td>Pyrus communis</td><td>pear</td>
<td>Ribes sylvestre</td><td>gooseberry</td>
<td>Ribes uva-crispa</td><td>currants</td>
<td>Ricinus communis</td><td>castor tree</td>
<td>Saccharum officinarum</td><td>sugar cane</td>
<td>Secale cereale</td><td>rye</td>
<td>Sesamum indicum</td><td>sesame</td>
<td>Solanum tuberosum</td><td>potatoes</td>
<td>Sorghum bicolor (s.vulgare)</td><td>sorghum</td>
<td>Sorghum dochna</td><td>sorghum sugar</td>
<td>Spinacia oleracea</td><td>spinach</td>
<td>Theobroma cacao</td><td>cocoa tree</td>
<td>Trifolium pratense</td><td>clover</td>
<td>Triticum aestivum</td><td>wheat</td>
<td>Triticum durum</td><td>durum wheat</td>
<td>Vaccinium corymbosum</td><td>bruise</td>
<td>Vaccinium vitis-idaea</td><td>lingonberry</td>
<td>Vicia faba</td><td>feed beans</td>
<td>Vigna sinensis (V.unguiculata)</td><td>vigna</td>
Lithuanian name for grape corn
Botanical name
Vitis vinifera
Zea mays
For broadening the spectrum of action and obtaining a synergistic effect, the cyclohexenone derivatives of Formula I may be mixed with each other or with other groups of biologically active agents with herbicidal or growth-regulating activity and co-production. For example, the component of the mixture may be diazines, 4H3, 1-benzoxazinine derivatives, benzothiadiazinones, 2,6-dinitroanilines, N-phenylcarbamates, thiolcarbamates, halo carbonic acids, triazines, amides, ureas, diphenyl ether, triazinones, uracil derivatives, benzofuran derivatives, , cyclohexenones, acids, (hetero) aryloxypropionic acids, amides, etc.
their salts, esters and esters
In addition, the cyclohexenone derivatives of formula I, or herbicidal compositions containing them, can be co-prepared, if desired, either in combination with other herbicides or in combination with plant protection products such as pests or phytopathogenic fungi or bacteria. Of interest continues to be the ability to combine with mineral salt solutions, which are introduced to increase nutrients and micronutrients. For this, additives are used in concentrates of non-phytotoxic oils and oils.
The following synthesis examples are used for the subsequent preparation of hydroxylamine of formula III and cyclohexenone oxime ether of formula I in the presence of the corresponding starting compounds; The physical properties of the compounds produced are shown in the tables below.
Synthesis Example for Hydroxylamine (III) (E) - 4-Bromo-1- (2-thienyl) -1-butene
Add 225 g (1.46 mol) of cyclopropyl-2-thienylcarbinol in 972 ml of 48% hydrobromic acid dropwise over a period of 1 hour at 5 to 10 ° C. After 2 hours at room temperature, the organic phase is separated and the aqueous phase is extracted three times with 300 ml of dichloromethane each time. The organics were washed with dilute sodium hydroxide and water until neutral, dried over MgSO 4<sub>4</sub> and concentrated in vacuo. 322 g (94% error) of wet bromide (GC: 92%) are obtained.
1 H-NMR (250 MHz,
3.46 (t, 2H),
CDC1<sub>3</sub>): Δ = 2, 65-2, 80 (m, 2H),
5.90-6.10 (m, 1H), 6.61 (d, 1H),
6.80-7.0 (m, 2H), 7.14 (d, 1H)
N - [(E) -4- (2-Thienyl) -3-butenyloxy] phthalimide
190 ml (1.37 mol) of triethylamine are added dropwise at 20-25 ° to a mixture of 283 g (1.30 mol) of the above bromide, 1300 ml of N-methyl-2-pyrrolidinone, 10 g in 2.5 hours. of potassium iodide and 212 g
<td>(1.30 mol) of N-hydroxyphthalimide.</td><td>After 4</td><td>hours</td><td>20-25 ° C</td>
<td>at temperature, the contents are discarded</td><td>to</td><td>4000 ml</td><td>icy</td>
<td>water and make up portions</td><td> 500</td><td>ml 10%</td><td>sodium</td>
<td>alkali.</td><td></td><td></td><td></td>
<td>Extract four times after</td><td> 500</td><td colspan="2">ml of ethyl acetate.</td>
The combined ethyl acetate phases are washed with dilute caustic soda and water until neutral, dried over MgSO 4<sub>4</sub> and concentrated in vacuo. The wet product is purified by chromatography on a 30 x 15 cm column over 1000 g of silica gel (solvent: n-hexane / dichloromethane 7: 3). 113 g (29%) of phthalimide ether with a flash point of 69-71 [deg.] C. (isopropane) are obtained.
<sup>1</sup>1 H-NMR (250 MHz, d<sub>6</sub> - DMSO): δ = 2.55-2, 70 (m, 2H),
4.28 (t, 2H), 6.00-6.20 (m, 1H), 6.77 (d, 1H), 7.00 (m, 2H), 7.35 (m, 1H), 7 , 87 (s, 4H).
O - [(E) -4- (2-Thienyl) -3-butenyl] hydroxylamine
A mixture of 90.2 g (0.30 mol) of the above phthalimide ether and 136 ml of ethanolamine is stirred for 3 hours at 60 ° C. The cooled reaction mixture is poured into 200 mL of ice water. Make up to 200 ml with saturated sodium chloride solution and extract three times with 300 ml of dichloromethane. The combined organic phases are washed three times with 100 ml of saturated sodium chloride solution, dried over MgSO<sub>4</sub> and concentrated in vacuo. 45 g (89%) of hydroxylamine are obtained.
1 H-NMR (250 MHz, CDCl 3)<sub>3</sub>): δ = 3.78 (t, 2H), 5.40 (pls 2H),
6.57 (d, 1H), 6.80-7.15 (m, 3H).
2.40-2.55 (m, 2H),
5, 96-6.20 (m, 1H),
Example of synthesis for the preparation of cyclohexenone oxime ether derivatives (I)
2- [1 - [[(E) -4- (2-Thienyl) -3-butenyloxy] imino] -butyl] -3-hydroxy-5- (2H-tetrahydropyran-4-yl) -2-cyclohexenone-1
A mixture of 35 g (0.13 mol) of 2-butyryl-3-hydroxy-5- (2H-tetrahydropyranyl-4) -2-cyclohexenone-1 and 24 g (0.14 mol)
O - [(E) -4- (2-Thienyl) -3-butenyl] hydroxylamine was stirred in 300 mL of methanol for 16 h. Concentrate in vacuo and pour into 1000 ml of 10% sodium hydroxide. Extract three times with 200 ml each of methylene chloride and, after cooling on ice, obtain a pH of 1 with concentrated hydrochloric acid. The aqueous phase is then extracted three times with 200 ml of ether and then dried.
MgSO<sub>4</sub> and concentrated in vacuo. The wet product is purified by chromatography on a 30 x 15 cm column on 1000 g of silica gel (solvent: ethyl acetate). 46 g (85 µs) of cyclohexenone oxime ether are obtained.
<sup>X</sup>1 H-NMR (200 MHz, CDCl 3)<sub>3</sub>): δ = 0.95 (t, 3H), 1.17-
<td> 1, 96</td><td>(m, 9H), 2113</td><td>(m, 1H), 2.36 (m, 1H),</td><td> 2,43-</td><td>-2.70 (m,</td>
<td>3H),</td><td>2.88 (m, 2H),</td><td>3.36 (t, 2H), 4.02 (d,</td><td>2H),</td><td>4.15 (t,</td>
<td>2H),</td><td>6.00 (dt, 1H)</td><td>, 6.60 (d, 1H), 6.80-</td><td> -7, 20</td><td>(m, 3H),</td>
<td> 14,75</td><td>(s, 1H).</td><td></td><td></td><td></td>
U o
-P
No. AZX n Physical Data BMR: mdlyd.
K
<td>LO</td><td></td><td></td><td></td><td></td>
<td>m</td><td></td><td></td><td></td><td> 3</td>
<td> •</td><td></td><td></td><td></td><td></td>
<td>Lf)</td><td>^ ~ k</td><td>»K</td><td></td><td>tn</td>
<td>K</td><td> 32</td><td></td><td></td><td>tn</td>
<td></td><td>t— <</td><td> 32</td><td></td><td></td>
<td>X</td><td>«K</td><td>OJ</td><td></td><td>kO</td>
<td>CM</td><td>ω</td><td>«K</td><td></td><td></td>
<td> *«</td><td></td><td>-P</td><td></td><td>* k</td>
<td>-P</td><td>o</td><td></td><td></td><td>X-month</td>
<td><sup>1</sup>—’</td><td>m</td><td> 00</td><td></td><td> 32</td>
<td>o</td><td>k</td><td>kO</td><td></td><td>I</td>
<td>Γ-</td><td>r-</td><td>* k</td><td></td><td></td>
<td> •</td><td>k</td><td>n</td><td></td><td>ε.</td>
<td>PO</td><td>«« —K</td><td></td><td>ζ — χ</td><td></td>
<td>• k</td><td> 32</td><td></td><td>X</td><td>ro</td>
<td>k</td><td>r-1</td><td></td><td>ro</td><td>o</td>
<td>Λ</td><td></td><td>X</td><td></td><td></td>
<td>OJ</td><td>e</td><td>CM</td><td>e</td><td>LO</td>
<td></td><td></td><td>K</td><td> *—'</td><td></td>
<td>-P</td><td>r-</td><td>-P</td><td>LO</td><td></td>
<td>-—R</td><td>OJ</td><td></td><td>rd</td><td></td>
<td></td><td>* k</td><td></td><td>k.</td><td>X</td>
<td></td><td>kO</td><td>Γ-</td><td>Γ-</td><td>i-1</td>
<td>co</td><td></td><td>ΟΟ</td><td>Ι</td><td>k</td>
<td>K</td><td></td><td>»K</td><td>LO</td><td></td>
<td>OJ</td><td> 32</td><td>Oops</td><td>r-</td><td></td>
<td></td><td>rd</td><td></td><td>• k</td><td></td>
<td></td><td>, k</td><td>«K</td><td>kO</td><td>tn</td>
<td>X</td><td>S</td><td>^ -k.</td><td></td><td>CTi</td>
<td>CM</td><td></td><td>χ:</td><td>v</td><td>k</td>
<td></td><td>o</td><td>OJ</td><td></td><td>tn</td>
<td> 3</td><td>o</td><td>k.</td><td> 32</td><td>k</td>
<td></td><td>«K</td><td>ε.</td><td>Oops</td><td>^ -k</td>
<td>o</td><td>kO</td><td></td><td>k.</td><td>K</td>
<td>o</td><td>xk</td><td>o</td><td>co</td><td>ro</td>
<td>«K</td><td> 32</td><td>k.</td><td>rp</td><td>K</td>
<td>OJ</td><td>OJ</td><td>OJ</td><td>a</td><td>co</td>
<td> 1</td><td> •</td><td> 1</td><td></td><td>• «—r</td>
<td>o</td><td>CO</td><td>LO</td><td>O</td><td>o</td>
<td> 00</td><td>»—I</td><td> 00</td><td>ro</td><td>tn</td>
<td>k.</td><td>Pi</td><td>«K</td><td></td><td>K</td>
<td>r-1</td><td></td><td>ri</td><td>Lf)</td><td>co</td>
<td>O</td><td>O</td><td>o</td><td>o</td><td>o</td><td>Fd</td><td>O</td><td>o</td><td>Fd</td><td>O</td>
<td></td><td></td><td></td><td></td><td></td><td>m</td><td></td><td></td><td>CO</td><td></td>
<td></td><td></td><td></td><td></td><td></td><td> 32</td><td></td><td></td><td> 32</td><td></td>
<td> 1</td><td> 1</td><td> 1</td><td> 1</td><td> 1</td><td>O</td><td> 1</td><td> 1</td><td>U 1</td><td> 1</td>
<td></td><td></td><td></td><td></td><td></td><td>1 M</td><td></td><td></td><td>tn</td><td></td>
<td>CM</td><td>CM 1</td><td>CM 1</td><td>CM</td><td>CM</td><td>CM</td><td>CM</td>
<td> 1</td><td>CO</td><td>CO</td><td> 1</td><td> 1</td><td> 1</td><td> 1</td>
<td>co</td><td> (0</td><td>(U</td><td>CO</td><td>CO</td><td>CO</td><td>CO</td>
<td> (0</td><td>i-1</td><td>r-1</td><td> (0</td><td>(ow</td><td>Φ</td><td> <0</td>
<td>rp</td><td>-H</td><td>• rd</td><td>r— (</td><td>-—T</td><td>«-D</td><td>rd</td>
<td>• rd</td><td>n</td><td>C</td><td>• H</td><td>-H</td><td>H</td><td>• P</td>
<td>c</td><td>H</td><td> (0</td><td>C</td><td>C</td><td>o</td><td>C</td>
<td>Φ</td><td>P</td><td>P</td><td>φ</td><td>Φ</td><td>P</td><td>Φ</td>
<td>Ή</td><td>H</td><td> 3</td><td>• H</td><td>Ή</td><td>• rd</td><td>• P</td>
<td>-P</td><td>CL</td><td>Ml</td><td> 4-)</td><td> 4-)</td><td>a</td><td> 4-»</td>
<td>CM</td><td>(N</td><td>CJ X o CM</td><td>CM X o CM</td>
<td>X</td><td>X</td><td>X</td><td>X</td>
<td>u</td><td>u</td><td>u</td><td>u</td>
<td>CM</td><td>CM</td><td>CM</td><td>CM</td>
<td>X</td><td>X</td><td>X</td><td>X</td>
<td>u</td><td>o</td><td>o</td><td>o</td>
<td>rd</td><td>CM</td><td>CO</td><td></td>
<td>O</td><td>O</td><td>o</td><td>o</td>
<td></td><td colspan="2">O <n</td><td>X u</td><td>X U</td>
<td>CM X u CM</td><td>CM X O CM</td><td>X u</td><td>m X u</td><td>co X o</td>
<td>X</td><td>X</td><td>X</td><td>X</td><td>X</td>
<td>o</td><td>U</td><td>o</td><td>u</td><td>o</td>
<td>CM</td><td>CM</td><td>CJ</td><td>CM</td><td>CM</td>
<td>X</td><td>X</td><td>X</td><td>X</td><td>X</td>
<td>u</td><td>o</td><td>u</td><td>o</td><td>o</td>
<td>tn</td><td>LO</td><td></td><td>ro</td><td>Ch</td>
<td>o</td><td>O</td><td>o</td><td>o</td><td>o</td>
-10 CH<sub>?</sub>CH-CH furanylLT 3295 B
CO
U o
-P
CO
No. AZX n Physical Data BMR: mdlyd.
<td colspan="2"> 3</td>
<td>m f-1</td><td></td>
<td>kO</td><td>K</td>
<td></td><td>. i-1</td>
<td></td><td>k</td>
<td>a</td><td>Ό</td>
<td>CN</td><td></td>
<td></td><td> 00</td>
<td>m</td><td>f-1</td>
<td>f-1</td><td> •</td>
<td> 0.</td><td>r-</td>
<td>m</td><td></td>
<td>ν '</td><td> 5?</td>
<td>K</td><td>CN</td>
<td>m</td><td></td>
<td></td><td>ε.</td>
<td></td><td>o</td>
<td>a</td><td>o</td>
<td>CN</td><td>K</td>
<td> .</td><td>r-</td>
<td>T)</td><td></td>
<td>τ)</td><td></td>
<td> -</td><td>a</td>
<td>CN</td><td> 1“1</td>
<td>n</td><td></td>
<td>k.</td><td>TJ</td>
<td></td><td></td>
<td colspan="2">-P</td>
<td>S</td><td></td>
<td></td><td>a</td>
<td> 00</td><td>i-1</td>
<td>o</td><td></td>
<td></td><td>S</td>
<td>kO</td><td>C-</td>
<td></td><td>r-</td>
<td></td><td></td>
<td>a</td><td>co</td>
<td colspan="2">CN</td>
<td>K</td><td>«K</td>
<td>w</td><td></td>
<td>r— |</td><td>a</td>
<td> 0.</td><td>r-1</td>
<td></td><td>K n</td>
<td> 00</td><td></td>
<td> 00</td><td>CN</td>
<td></td><td>r-</td>
<td>m</td><td>co</td>
<td colspan="2"> *»</td>
<td></td><td></td>
<td>a</td><td></td>
<td>CN</td><td>X</td>
<td>K</td><td>i-1</td>
<td>Ό</td><td></td>
<td>n</td><td>Ί3</td>
<td>• c · - *</td><td></td>
<td>CN</td><td>cn</td>
<td>n</td><td>co</td>
<td></td><td> •</td>
<td>'sr</td><td>co</td>
<td>o</td><td>M</td><td>M</td><td>M</td><td>o</td><td>o</td><td>o</td><td> 1-1</td><td>M</td><td>O</td>
<td></td><td>r-1</td><td>en X</td><td>M</td><td></td><td></td><td></td><td>r- |</td><td>n a</td><td></td>
<td> 1</td><td>U 1</td><td>u</td><td>CQ I</td><td> 1</td><td> 1</td><td> 1</td><td>O |</td><td>u |</td><td> 1</td>
<td></td><td>m</td><td>1 LT)</td><td> *3*</td><td></td><td></td><td></td><td>m</td><td>1 LO</td><td></td>
<td colspan="2"></td><td colspan="4">m</td><td colspan="4">CN</td>
<td>CN 1</td><td>CN 1</td><td>CN 1</td><td>m 1</td><td>l co</td><td></td><td>1 co</td><td></td><td></td><td>m 1</td>
<td>CO</td><td>CO</td><td>co</td><td>co</td><td> «3</td><td>I</td><td>(U</td><td>I</td><td> 1</td><td>co</td>
<td> (0</td><td> (0</td><td></td><td> (0</td><td>r - l</td><td></td><td> •—1</td><td></td><td></td><td>oh</td>
<td>r-1</td><td>i-1</td><td> 1—1</td><td>i-1</td><td>-H</td><td>η</td><td>• P</td><td> *|</td><td> *1</td><td><—I</td>
<td>• P</td><td>Ή</td><td>• ri</td><td>• H</td><td></td><td></td><td>c</td><td></td><td></td><td>-P</td>
<td>C</td><td>C</td><td>c</td><td>C</td><td>• rd</td><td></td><td>d)</td><td></td><td></td><td>c</td>
<td>d)</td><td>d)</td><td>d)</td><td>d)</td><td></td><td></td><td>• P</td><td></td><td></td><td>d)</td>
<td>• H</td><td>• H</td><td>• P</td><td>• H</td><td>• H</td><td></td><td>P</td><td></td><td></td><td>P</td>
<td>-P</td><td>-P</td><td>-P</td><td>-P</td><td>cx</td><td></td><td>-P</td><td></td><td></td><td>-P</td>
hi
ia
ui
K u
i
K
Oh i
<td>a</td><td>a</td><td>a</td><td>a</td><td>a</td><td>a</td><td>cn</td><td>co</td><td><n</td><td>m</td>
<td>o</td><td>o</td><td>u</td><td>u</td><td>u</td><td>u</td><td>a</td><td>a</td><td>a</td><td>a</td>
<td> 1</td><td> 1</td><td> 1</td><td> 1</td><td> 1</td><td> 1</td><td>u</td><td>o</td><td>υ</td><td>u</td>
<td>a</td><td>a</td><td>a</td><td>a</td><td>a</td><td>a</td><td> —*</td><td> ·*-</td><td>Τ ''</td><td> *</td>
<td>o</td><td>o</td><td>u</td><td>u</td><td>u</td><td>υ</td><td>u</td><td>u</td><td>υ</td><td>u</td>
<td>CN</td><td>CN</td><td>CN</td><td>CN</td><td>CM</td><td>CN</td><td>CM</td><td>CM</td><td>CM</td><td>CM</td>
<td>a</td><td>a</td><td>a</td><td>a</td><td>a</td><td>a</td><td>a</td><td>a</td><td>a</td><td>a</td>
<td>u</td><td>u</td><td>a</td><td>o</td><td>u</td><td>o</td><td>u</td><td>o</td><td>u</td><td>u</td>
<td>M</td><td>CN</td><td>n</td><td></td><td>m</td><td>co</td><td>r-</td><td> 00</td><td>cn</td><td>O</td>
<td>ll</td><td>i-1</td><td>i-1</td><td> 1—1</td><td>i-1</td><td>i-1</td><td>i-1</td><td>f-1</td><td>i-l</td><td>CN</td>
.21 CH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub> furanyl-2- 0.1, 50-1.80 (m, 4H), 2.64 (t, 2H), 3.68 (t, 2H), 5.35 (pls, 2H), 5.97 (m , 1H), 6.18 (m, 1H), 7.30 (s, 1H)
No. AZX n Physical Data BMR: mdlyd.
<td></td><td colspan="4">00 kO</td><td colspan="2"></td><td colspan="2">o</td><td colspan="3">re</td>
<td></td><td></td><td></td><td>he</td><td></td><td>X</td><td></td><td></td><td></td><td>r-4</td><td></td><td></td>
<td></td><td></td><td></td><td>en</td><td></td><td></td><td></td><td>LO</td><td></td><td>he</td><td>he</td><td></td>
<td></td><td></td><td></td><td></td><td></td><td>he</td><td></td><td></td><td></td><td> 3</td><td>χ— ».</td><td></td>
<td></td><td>he</td><td></td><td>he</td><td></td><td> £</td><td></td><td>he</td><td></td><td></td><td>re</td><td></td>
<td></td><td>X - k</td><td></td><td>χ — χ</td><td></td><td></td><td></td><td>X</td><td></td><td>m</td><td>CM</td><td></td>
<td></td><td>X</td><td></td><td>X</td><td></td><td>o</td><td></td><td>re</td><td></td><td>Lf)</td><td>he</td><td></td>
<td></td><td>CM</td><td></td><td>CM</td><td></td><td> 00</td><td></td><td>CM</td><td></td><td>he</td><td>co</td><td></td>
<td></td><td></td><td></td><td>he</td><td></td><td>he</td><td>x— «.</td><td>he</td><td></td><td>kO</td><td> »-4</td><td></td>
<td></td><td>-P</td><td></td><td>-P</td><td></td><td>CM</td><td>re</td><td>-P</td><td></td><td></td><td> 3</td><td></td>
<td></td><td></td><td></td><td></td><td></td><td> 1</td><td>CM</td><td></td><td></td><td>he</td><td></td><td></td>
<td></td><td>c-1</td><td></td><td>kO</td><td></td><td>O</td><td>he</td><td>to</td><td></td><td>X ^</td><td>o</td><td></td>
<td></td><td></td><td></td><td>r-</td><td></td><td>Γ *</td><td>co</td><td>co</td><td></td><td></td><td>M<sup>1</sup></td><td></td>
<td></td><td>he</td><td></td><td>he</td><td>Χ-Χ.</td><td>he</td><td> -***</td><td>he</td><td></td><td>t-4</td><td>he</td><td></td>
<td></td><td>n</td><td></td><td>CM</td><td>re</td><td>CM</td><td>r *</td><td>co</td><td>re</td><td>he</td><td>LO</td><td></td>
<td></td><td></td><td></td><td></td><td>CM</td><td></td><td>r *</td><td></td><td>r-4</td><td> £</td><td></td><td></td>
<td></td><td>he</td><td></td><td>he</td><td>t,</td><td></td><td> <.</td><td>he</td><td>he</td><td></td><td>he</td><td></td>
<td></td><td>χ-χ</td><td>X</td><td></td><td>co</td><td></td><td>kO</td><td>X</td><td> 3</td><td>co</td><td>X</td><td>χ.</td>
<td></td><td>X</td><td>cn</td><td>X</td><td><sup>r</sup></td><td>X</td><td></td><td>re</td><td></td><td>o</td><td>re</td><td>re</td>
<td></td><td>CM</td><td>he</td><td>co</td><td>M<sup>1</sup></td><td></td><td>• k</td><td>CM</td><td> <33</td><td>he</td><td>CM</td><td> 1“4</td>
<td></td><td>he</td><td></td><td></td><td>LT)</td><td>he</td><td>X</td><td>he</td><td>Ό</td><td>kO</td><td></td><td>he</td>
<td></td><td>-P</td><td></td><td>C0</td><td>he</td><td> 3</td><td>X</td><td>-P</td><td>he</td><td></td><td>-P</td><td>co</td>
<td></td><td></td><td>O</td><td> —*</td><td>kO</td><td></td><td>CM</td><td></td><td>kO</td><td>he</td><td></td><td> -—*</td>
<td></td><td></td><td>CM</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td>
<td></td><td></td><td>he</td><td>CO</td><td>he</td><td>o</td><td>κ</td><td></td><td>he</td><td>X</td><td> 00</td><td>o</td>
<td></td><td> 00</td><td>r-</td><td></td><td></td><td> 00</td><td>CO</td><td>r ^</td><td>X.</td><td>i-4</td><td>r-</td><td>co</td>
<td></td><td>he</td><td> 1</td><td>he</td><td> 04</td><td>he</td><td>«—I</td><td>he</td><td>you</td><td>he</td><td>he</td><td>he</td>
<td></td><td>CM</td><td>o</td><td>CM</td><td>CM</td><td>r-1</td><td>Oh,</td><td>CM</td><td>i-4</td><td></td><td>co</td><td>r-</td>
<td></td><td></td><td></td><td></td><td> *»</td><td> 1</td><td></td><td></td><td>he</td><td></td><td></td><td></td>
<td></td><td>he</td><td>he</td><td>he</td><td>to</td><td>o</td><td>o</td><td>he</td><td>T5</td><td>IG</td><td>he</td><td>he</td>
<td></td><td></td><td>kO</td><td>x- ^</td><td>1-e</td><td>LT)</td><td>co</td><td>X</td><td> -—</td><td>ΟΊ</td><td></td><td></td>
<td></td><td>X</td><td></td><td>X</td><td> 3</td><td>he</td><td>he</td><td>X</td><td>in</td><td>he</td><td>re</td><td>X</td>
<td></td><td><g «</td><td>he</td><td></td><td></td><td>r-4</td><td>LO</td><td>KT</td><td>m</td><td>LO</td><td>CM</td><td></td>
<td></td><td>he</td><td>s— *.</td><td></td><td>o</td><td></td><td></td><td>he</td><td> <</td><td></td><td>he</td><td>he</td>
<td></td><td>e</td><td>X</td><td>ε</td><td>en</td><td>he</td><td>he</td><td>ε</td><td>Ό</td><td>he</td><td>ε.</td><td>, ε</td>
<td></td><td></td><td>CM</td><td></td><td></td><td>X</td><td>X— »</td><td> —’</td><td></td><td>χ</td><td></td><td></td>
<td></td><td>LT)</td><td>he</td><td>o</td><td>m</td><td>re</td><td>X</td><td>o</td><td></td><td>re</td><td>o</td><td>o</td>
<td></td><td> 00</td><td>m</td><td> 00</td><td></td><td>CM</td><td>CM</td><td> 00</td><td></td><td>CO</td><td>L0</td><td>LO</td>
<td></td><td>he</td><td>r-1</td><td>he</td><td></td><td>he</td><td>he</td><td> *.</td><td>re</td><td>he</td><td></td><td>he</td>
<td></td><td>r-1</td><td>Qę</td><td>r<sup>-</sup>1</td><td></td><td>-P</td><td>-P</td><td>r - t</td><td>CM</td><td>co</td><td>CM</td><td>kO</td>
<td></td><td> 1</td><td></td><td> 1</td><td>re</td><td></td><td></td><td> 1</td><td></td><td>• ta - * -</td><td> 1</td><td> 1</td>
<td></td><td>o</td><td>O</td><td>IO</td><td>CM</td><td>Γ '</td><td>O</td><td>o</td><td>n</td><td>o</td><td>O</td><td>o</td>
<td></td><td>tO</td><td>en</td><td>and></td><td></td><td>CM</td><td></td><td>m</td><td>i-1</td><td>LO</td><td>M<sup>1</sup></td><td>o</td>
<td></td><td>he</td><td>he</td><td>he</td><td>-P</td><td></td><td> «.</td><td></td><td>b,</td><td>he</td><td></td><td>he</td>
<td></td><td>r-1</td><td>m</td><td>r4</td><td></td><td>τ-1</td><td>co</td><td>r - t</td><td></td><td>CO</td><td>CM</td><td>kO</td>
<td>M</td><td>o</td><td></td><td>H4</td><td></td><td>t - t</td><td></td><td>(p</td><td></td><td> 1-4</td><td>O</td><td></td>
<td>n K</td><td></td><td></td><td>ΠΊ X</td><td></td><td rowspan="2">m re CM υ</td><td></td><td>i-1</td><td></td><td><n X</td><td></td><td></td>
<td>u I</td><td> 1</td><td></td><td>u |</td><td></td><td></td><td>O l</td><td></td><td>u</td><td> 1</td><td></td>
<td>LT)</td><td></td><td></td><td>LO</td><td></td><td>m</td><td></td><td>LD</td><td></td><td>i-4</td><td></td><td></td>
<td>CM 1</td><td>CM</td><td></td><td>CM</td><td></td><td>CM</td><td></td><td>CM</td><td></td><td>CM 1</td><td>CM 1</td><td></td>
<td>n</td><td> 1</td><td></td><td> 1</td><td></td><td> 1</td><td></td><td> 1</td><td></td><td>en</td><td>en</td><td></td>
<td> (0</td><td>en</td><td></td><td>CQ</td><td></td><td>co</td><td></td><td>en</td><td></td><td><TJ</td><td>(U</td><td></td>
<td>I - Vol</td><td> «3</td><td></td><td><TJ</td><td></td><td>Π3</td><td></td><td> (0</td><td></td><td>i-t</td><td> 1-1</td><td></td>
<td>• H</td><td>i-1</td><td></td><td>i-1</td><td></td><td><—T</td><td></td><td>i-t</td><td></td><td>-P</td><td>• P</td><td></td>
<td>C</td><td>• H</td><td></td><td>-rt</td><td></td><td>P</td><td></td><td>-P</td><td></td><td>rp</td><td>c</td><td></td>
<td> (0</td><td>C</td><td></td><td>C</td><td></td><td>c</td><td></td><td>C</td><td></td><td>O</td><td>you)</td><td></td>
<td>p</td><td>Φ</td><td></td><td>d)</td><td></td><td>Φ</td><td></td><td>Φ</td><td></td><td>P</td><td>P</td><td></td>
<td> 3</td><td>• H</td><td></td><td>• P</td><td></td><td>P</td><td></td><td>-P</td><td></td><td>-P</td><td> 3</td><td></td>
<td> 4-1</td><td>-P</td><td></td><td>-P</td><td></td><td>-P</td><td></td><td>-P</td><td></td><td>a</td><td>LP</td><td></td>
<td>(N</td><td>CM</td><td></td><td>CM</td><td></td><td>CM</td><td></td><td>CM</td><td></td><td>CM</td><td></td><td></td>
<td>m</td><td>re</td><td></td><td>re</td><td></td><td>re</td><td></td><td>re</td><td></td><td>re</td><td>re</td><td></td>
<td>u</td><td>u</td><td></td><td>υ</td><td></td><td>υ</td><td></td><td>L></td><td></td><td>u</td><td>u</td><td></td>
<td>CM</td><td>CM</td><td></td><td>CM</td><td></td><td>CM</td><td></td><td>CM</td><td></td><td>CM</td><td> 1</td><td></td>
<td>K</td><td>re</td><td></td><td>re</td><td></td><td>re</td><td></td><td>re</td><td></td><td>re</td><td>re</td><td></td>
<td>U</td><td>u</td><td></td><td>o</td><td></td><td>υ</td><td></td><td>u</td><td></td><td>u</td><td>u</td><td></td>
<td>CM</td><td>CM</td><td></td><td>CM</td><td></td><td>CM</td><td></td><td>CM</td><td></td><td>CM</td><td>CM</td><td></td>
<td>X</td><td>X</td><td></td><td>re</td><td></td><td>re</td><td></td><td>re</td><td></td><td>re</td><td>re</td><td></td>
<td>O</td><td>o</td><td></td><td>o</td><td></td><td>u</td><td></td><td>u</td><td></td><td>o</td><td>u</td><td></td>
<td>CM</td><td>CM</td><td></td><td>CM</td><td></td><td>CM</td><td></td><td>CM</td><td></td><td>CM</td><td>CM</td><td></td>
<td>re</td><td>X</td><td></td><td>re</td><td></td><td>re</td><td></td><td>re</td><td></td><td>re</td><td>re</td><td></td>
<td>u</td><td>u</td><td></td><td>u</td><td></td><td>o</td><td></td><td>u</td><td></td><td>o</td><td>u</td><td></td>
<td>CM</td><td>ro</td><td></td><td>'T</td><td></td><td>LO</td><td></td><td>Ό</td><td></td><td>r ~</td><td> 00</td><td></td>
<td>CM</td><td>CM</td><td></td><td>CM</td><td></td><td>CM</td><td></td><td>CM</td><td></td><td>CM</td><td>CM</td><td></td>
<td> •</td><td> •</td><td></td><td> •</td><td></td><td> •</td><td></td><td> •</td><td></td><td></td><td> •</td><td></td>
.29 CH<sub>2</sub>CH<sub>2</sub>CH-CH furanyl-3-0 2.40-2.55 (m, 2H), 3.76 (t, 2H), 5.40 (bs, 2H), 5.856.05 (m, 1H), 6, 33 (d, 1H), 6.52 (s, 1H), 7.30-7.45 (m, 2H)
No. AZX n Physical Data BMR: mdlyd.
II
<td colspan="4">LO CTi</td><td colspan="4">1 o</td><td colspan="7">O O</td>
<td>fe</td><td></td><td></td><td></td><td></td><td></td><td>o</td><td></td><td>fe</td><td></td><td></td><td>, —Fe</td><td></td><td></td><td></td>
<td>tn</td><td></td><td></td><td></td><td></td><td></td><td>fe</td><td></td><td>LD</td><td></td><td></td><td>X</td><td></td><td></td><td></td>
<td></td><td></td><td>fe</td><td></td><td>fe</td><td></td><td>LD</td><td></td><td></td><td></td><td>fe</td><td>CN</td><td></td><td></td><td></td>
<td>fe</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>fe</td><td></td><td>X-fe</td><td>fe</td><td></td><td></td><td></td>
<td></td><td></td><td>ac</td><td></td><td>ac</td><td></td><td>K</td><td></td><td></td><td></td><td>X</td><td>ε</td><td></td><td></td><td></td>
<td>K</td><td></td><td>CN</td><td></td><td>CN</td><td></td><td>, —X</td><td></td><td>□ c</td><td></td><td>CM</td><td></td><td></td><td></td><td></td>
<td>CN</td><td>ac</td><td>fe</td><td></td><td>fe</td><td></td><td>ra</td><td>ac</td><td>CM</td><td>ac</td><td></td><td>o</td><td></td><td></td><td></td>
<td>fe</td><td>co</td><td>n</td><td></td><td>cn</td><td></td><td>CM</td><td>co</td><td>fe</td><td>CN</td><td>W</td><td>rH</td><td></td><td></td><td></td>
<td>m</td><td></td><td>rH</td><td></td><td><—H</td><td></td><td>fe</td><td>fe</td><td>W</td><td>fe</td><td>rH</td><td>fe</td><td></td><td></td><td></td>
<td>Λ</td><td> 3</td><td>O</td><td></td><td>a,</td><td></td><td>CO</td><td>ε</td><td> 33</td><td>ε</td><td>cu</td><td>r ·</td><td></td><td></td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td> 33</td><td>fe · * »</td><td></td><td></td><td></td><td> 1</td><td></td><td></td><td></td>
<td>o</td><td>tn</td><td>o</td><td></td><td>o</td><td></td><td></td><td>o</td><td>O</td><td>o</td><td>o</td><td>o</td><td></td><td></td><td></td>
<td>M *</td><td>rH</td><td></td><td></td><td></td><td></td><td>o</td><td>CO</td><td></td><td>rH</td><td>M *</td><td> 00</td><td></td><td>ac</td><td>ac</td>
<td>fe</td><td>fe</td><td></td><td></td><td>fe</td><td>S</td><td></td><td>fe</td><td>fe</td><td>fe</td><td>fe</td><td>fe</td><td></td><td>rH</td><td>rH</td>
<td>m</td><td>r *</td><td>m</td><td>ac</td><td>tn</td><td>ac</td><td>fe</td><td>r *</td><td>tn</td><td></td><td>LO</td><td>to</td><td></td><td>fe</td><td>fe</td>
<td></td><td> 1</td><td></td><td>co</td><td></td><td>co</td><td>LD</td><td> 1</td><td></td><td> 1</td><td></td><td></td><td></td><td>cn</td><td>ε</td>
<td>fe</td><td>o</td><td></td><td></td><td>fe</td><td>fe</td><td></td><td>o</td><td>fe</td><td>o</td><td>fe</td><td>fe</td><td></td><td></td><td></td>
<td></td><td> 00</td><td></td><td> £</td><td></td><td></td><td></td><td>o</td><td></td><td>cn</td><td>X * fe</td><td><* »Fe</td><td></td><td>o</td><td>o</td>
<td>ac</td><td>fe</td><td>ac</td><td></td><td>ac</td><td></td><td></td><td>fe</td><td>ac</td><td>K</td><td>ac</td><td>ac</td><td>X</td><td>co</td><td>rH</td>
<td>CN</td><td>LD</td><td>CN</td><td>o</td><td>CN</td><td>o</td><td>ac</td><td>r-</td><td>CN</td><td>tD</td><td>CM</td><td>rH</td><td>co</td><td> «»</td><td>fe</td>
<td>fe</td><td></td><td></td><td>r *</td><td>b »</td><td> 00</td><td>CM</td><td></td><td>fe</td><td></td><td>fe</td><td>fe</td><td> ·»</td><td>r-</td><td></td>
<td>-P</td><td>k</td><td>P</td><td>fe</td><td>-U</td><td>fe</td><td>fe</td><td></td><td>4J</td><td>fe</td><td>-P</td><td>Ό</td><td>ε</td><td></td><td></td>
<td></td><td></td><td></td><td>LD</td><td></td><td>LD</td><td>P</td><td></td><td></td><td></td><td>feo *</td><td></td><td></td><td>fe</td><td>fe</td>
<td></td><td>OG</td><td></td><td> 1</td><td></td><td> 1</td><td></td><td>ac</td><td></td><td>ac</td><td></td><td></td><td></td><td>* -fe »</td><td>* -fe</td>
<td> 00</td><td>rH</td><td>tn</td><td>O</td><td></td><td>O</td><td></td><td>rH</td><td>O</td><td>rH</td><td> 00</td><td>CN</td><td>LD</td><td>ac</td><td>ac</td>
<td>r-</td><td>fe</td><td>r-</td><td></td><td>r-</td><td></td><td>o</td><td>fe</td><td> 00</td><td>fe</td><td>r *</td><td>CD</td><td>rH</td><td>rH</td><td>rH</td>
<td>fe</td><td>S</td><td>fe</td><td></td><td></td><td>fe</td><td> 00</td><td>S</td><td>fe</td><td>S</td><td>fe</td><td>fe</td><td>fe</td><td>fe</td><td>fe</td>
<td>co</td><td></td><td>co</td><td>LD</td><td>co</td><td>LD</td><td>fe</td><td></td><td>co</td><td></td><td>co</td><td>LD</td><td>Γ *</td><td>ε.</td><td>ε.</td>
<td></td><td></td><td></td><td></td><td></td><td></td><td>co</td><td></td><td></td><td></td><td></td><td></td><td> 1</td><td></td><td></td>
<td>M</td><td>r-</td><td> *</td><td>fe</td><td>fe</td><td> %</td><td></td><td> 00</td><td>fe</td><td>o</td><td>fe</td><td>fe</td><td>o</td><td>o</td><td>o</td>
<td></td><td>m</td><td></td><td></td><td></td><td></td><td>fe</td><td></td><td>χ-fe</td><td>tn</td><td></td><td>X-fe</td><td> 00</td><td>CM</td><td>σι</td>
<td>ac</td><td></td><td>ac</td><td>ac</td><td>ac</td><td>3G</td><td>ac</td><td>fe</td><td>ac</td><td>K</td><td>ac</td><td>ac</td><td>fe</td><td>fe</td><td>fe</td>
<td>CN</td><td>tD</td><td>m</td><td>rH</td><td>CN</td><td>rH</td><td>CN</td><td>LD</td><td>CM</td><td>to</td><td>CM</td><td>rH</td><td>LD</td><td>LD</td><td>to</td>
<td>K</td><td></td><td></td><td>fe</td><td>fe</td><td>fe</td><td>fe</td><td></td><td>fe</td><td></td><td>fe</td><td>fe</td><td></td><td></td><td></td>
<td> 3</td><td>fe</td><td> 3</td><td> 3</td><td>ε_</td><td>e</td><td>ε</td><td>fe</td><td>ε</td><td>fe</td><td>ε</td><td>ε</td><td>fe</td><td>fe</td><td>fe</td>
<td></td><td></td><td></td><td></td><td></td><td> *—*</td><td></td><td></td><td> ’*—*</td><td></td><td></td><td></td><td></td><td> ,«««,,</td><td></td>
<td>tn</td><td>ac</td><td>tn</td><td>o</td><td>tn</td><td>o</td><td>tn</td><td>ac</td><td>o</td><td>ac</td><td>tn</td><td>o</td><td>ac</td><td>K</td><td>ac</td>
<td>tn</td><td>rH</td><td>tn</td><td>o</td><td>tn</td><td>rH</td><td>tn</td><td>rH</td><td>tD</td><td>rH</td><td>tn</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td>
<td>fe</td><td>fe</td><td>fe</td><td>fe</td><td>fe</td><td>fe</td><td>fe</td><td>fe</td><td>fe</td><td>fe</td><td>fe</td><td>fe</td><td>fe</td><td>fe</td><td>v</td>
<td>CM</td><td> &</td><td>CM</td><td>LD</td><td>CM</td><td>LD</td><td>CM</td><td> 3</td><td>CN</td><td>ε.</td><td>CN</td><td>to</td><td>ε</td><td>ε</td><td>ε</td>
<td>I</td><td></td><td> |</td><td> |</td><td> |</td><td> 1</td><td> 1</td><td></td><td> 1</td><td></td><td> 1</td><td> 1</td><td>fe *</td><td>'fe- »'</td><td>fe - »*</td>
<td>O</td><td>o</td><td>tn</td><td>O</td><td>LO</td><td>O</td><td>O</td><td>tn</td><td>O</td><td>o</td><td> 00</td><td>o</td><td>tn</td><td>r *</td><td>o</td>
<td></td><td>CN</td><td>m</td><td> 00</td><td>C0</td><td> 00</td><td></td><td>rH</td><td>'T</td><td>CN</td><td>r-1</td><td>σι</td><td>CN</td><td>σ »</td><td> 00</td>
<td>fe</td><td>fe</td><td></td><td>fe</td><td></td><td>fe</td><td>fe</td><td>fe</td><td>fe</td><td>fe</td><td>K</td><td>fe</td><td>fe</td><td>fe</td><td>fe</td>
<td>CM</td><td>tO</td><td>CM</td><td>tn</td><td>CM</td><td>uo</td><td>CN</td><td>LD</td><td>CM</td><td>to</td><td>CN</td><td>tn</td><td>tn</td><td>tn</td><td>to</td>
<td>O</td><td></td><td>1H</td><td></td><td>1H</td><td></td><td>O</td><td></td><td>1H</td><td></td><td>M</td><td></td><td>O</td><td>O</td><td>O</td>
-J<sup>1</sup> , - | i-I i-I o υ, uu γ i<sup>1</sup> ι im tn you are in
<td>CN</td><td>CN</td><td>CN</td><td>ro</td><td>ro</td><td>ro</td><td>CN</td><td>CN 1</td><td>CN</td>
<td> 1</td><td> 1</td><td> 1</td><td> 1</td><td> 1</td><td>l</td><td> 1</td><td>tn</td><td> 1</td>
<td>n</td><td>m</td><td> 05</td><td>CQ</td><td> 05</td><td>m</td><td> 05</td><td>(fl</td><td>to</td>
<td>(fl</td><td> <0</td><td><fl</td><td> (0</td><td> (0</td><td>(U</td><td>(fl</td><td>i-1</td><td> (0</td>
<td>i-1</td><td>i-1</td><td>> —T</td><td> «—1</td><td> <—1</td><td>i-t</td><td>i-t</td><td>• P</td><td> '—1</td>
<td>• H</td><td>-H</td><td>Ή</td><td>-H</td><td>• H</td><td>-H</td><td>• H</td><td>c</td><td>• P</td>
<td>C</td><td>C</td><td>C</td><td>G</td><td>C</td><td>G</td><td>C</td><td>(fl</td><td>G</td>
<td>fl)</td><td> 0)</td><td> 0)</td><td>fl)</td><td>fl)</td><td>fl)</td><td> 0)</td><td>P</td><td>fl)</td>
<td>-H</td><td>• H</td><td>H</td><td>H</td><td>-H</td><td>• P</td><td>• H</td><td>G</td><td>P</td>
<td>P</td><td>P</td><td>P</td><td>P</td><td>P</td><td>P</td><td>P</td><td>Mt.</td><td>P</td>
<td>ac</td><td>ac</td><td>ac</td><td>ac</td><td>ac</td><td>ac</td><td>n ac u</td><td>CN ac u CM ac</td><td>CN ac o CM ac</td>
<td>o</td><td>o</td><td>u</td><td>u</td><td>o</td><td>u</td><td>o</td><td>o</td><td>u</td>
<td> 1</td><td> 1</td><td> 1</td><td> 1</td><td> 1</td><td> 1</td><td> 1</td><td>CM</td><td>CM</td>
<td>ac</td><td>ac</td><td>ac</td><td>ac</td><td>ac</td><td>ac</td><td>ac</td><td>ac</td><td>ac</td>
<td>u</td><td>u</td><td>u</td><td>O</td><td>u</td><td>u</td><td>u</td><td>u</td><td>u</td>
<td>cn</td><td>CN</td><td>CN</td><td>CM</td><td>CN</td><td>CN</td><td>CM</td><td>CM</td><td>CM</td>
<td>ac</td><td>ac</td><td>ac</td><td>ac</td><td>ac</td><td>ac</td><td>ac</td><td>ac</td><td>ac</td>
<td>u</td><td>u</td><td>u</td><td>υ</td><td>o</td><td>u</td><td>u</td><td>o</td><td>u</td>
<td>CN</td><td>CN</td><td>CN</td><td>CM</td><td>CN</td><td>(N</td><td>CM</td><td>CM</td><td>CM</td>
<td>ac</td><td>ac</td><td>ac</td><td>ac</td><td>ac</td><td>ac</td><td>ac</td><td>ac</td><td>ac</td>
<td>u</td><td>u</td><td>u</td><td>u</td><td>u</td><td>u</td><td>u</td><td>o</td><td>u</td>
<td>O</td><td>rH</td><td>CM</td><td> 00</td><td>M *</td><td>m</td><td>LD</td><td>r-</td><td> 00</td>
<td>co</td><td>CO</td><td>CO</td><td>CO</td><td>CO</td><td>CO</td><td>CO</td><td>co</td><td>CO</td>
<td> •</td><td> •</td><td> •</td><td> •</td><td> «</td><td> •</td><td> »</td><td> •</td><td> •</td>
<td>1H</td><td>1H</td><td>1H</td><td>1H</td><td>hH</td><td>M</td><td>hH</td><td>hH</td><td>hH</td>
No. AZX n Physical Data BMR: mdlyd.
<td></td><td></td><td></td><td></td>
<td>Ή</td><td></td><td></td><td>K</td>
<td>r-1</td><td></td><td></td><td>rd</td>
<td>k</td><td></td><td></td><td>k</td>
<td>e</td><td></td><td></td><td>g</td>
<td></td><td></td><td></td><td> —*</td>
<td>m</td><td></td><td></td><td>Lf)</td>
<td>Lf)</td><td></td><td></td><td>lf)</td>
<td>k</td><td></td><td></td><td>k</td>
<td>uo</td><td></td><td></td><td>to</td>
<td>k</td><td></td><td></td><td>k</td>
<td>y— ».</td><td></td><td>^ you.</td><td></td>
<td>man</td><td>man</td><td>man</td><td>man</td>
<td>r "1</td><td>rd</td><td>r<sup>-</sup>1</td><td>rd</td>
<td>k</td><td>k</td><td>k</td><td>k</td>
<td>e</td><td>ω</td><td>g</td><td>g</td>
<td>k- * '</td><td></td><td></td><td> **-</td>
<td>n</td><td>o</td><td> ></td><td>co</td>
<td>o</td><td> 00</td><td>o</td><td>o</td>
<td>k</td><td>k</td><td>you.</td><td>k</td>
<td>kO</td><td>r-</td><td>r-</td><td>kO</td>
<td>k</td><td>k</td><td>k</td><td>k</td>
<td>^ -you »</td><td></td><td>you *</td><td>> —You *</td>
<td>man</td><td>X</td><td>man</td><td>man</td>
<td>r "1</td><td>i-H</td><td>r ~ 4</td><td>rd</td>
<td>k</td><td>k</td><td>k</td><td>k</td>
<td>g.</td><td>g.</td><td>g</td><td>g</td>
<td></td><td></td><td></td><td></td>
<td>m</td><td>o</td><td>o</td><td>Lf)</td>
<td>σι</td><td>CM</td><td><x></td><td>CM</td>
<td>k</td><td>k</td><td>k</td><td>k</td>
<td>Lf)</td><td>k £></td><td>kO</td><td>UO</td>
<td>k</td><td></td><td>k</td><td>k</td>
<td></td><td>k</td><td>you</td><td>X — you.</td>
<td>X</td><td>man</td><td>cc</td><td>man</td>
<td>co</td><td>T-1</td><td>rd</td><td>cn</td>
<td>k</td><td>k</td><td></td><td>k</td>
<td>ω</td><td>Him</td><td>e</td><td>cn</td>
<td></td><td></td><td></td><td> -</td>
<td>o</td><td>o</td><td>r-</td><td>o</td>
<td>Lf)</td><td>o</td><td> ></td><td>lf)</td>
<td>k</td><td>k</td><td>k</td><td>k</td>
<td>Uh</td><td>uo</td><td>UO</td><td>m</td>
<td>O</td><td>O</td><td>O</td><td>O</td>
<td>(* l</td><td></td><td></td><td>m</td>
<td>man</td><td></td><td></td><td>man</td>
<td>O <</td><td> 1</td><td> 1</td><td>U J</td>
<td>1 id</td><td></td><td></td><td>lG</td>
<td>CM 1</td><td>CM 1</td><td>CM</td><td>CM 1</td>
<td>cn</td><td>cn</td><td> 1</td><td>cn</td>
<td> (0</td><td>cti</td><td>cn</td><td><ti</td>
<td>r — I</td><td>»—T</td><td>(i.e.</td><td>i-1</td>
<td>-G</td><td>• H</td><td> 1—(</td><td>• G</td>
<td>i-C</td><td>G</td><td>• G</td><td>i-L</td>
<td> 0</td><td> (0</td><td>C</td><td>O</td>
<td>G</td><td>G</td><td>(D</td><td>G</td>
<td>• G</td><td>G</td><td>-G</td><td>G</td>
<td>Ch</td><td>Mg</td><td> 4-></td><td>Ol</td>
<td></td><td>Cl</td><td>CJ</td><td>Cl</td>
<td></td><td>man</td><td>man</td><td>man</td>
<td></td><td>o</td><td>U</td><td>u</td>
<td>d</td><td>CL</td><td>CJ</td><td>CJ</td>
<td>man</td><td>man</td><td>man</td><td>man</td>
<td>U</td><td>O</td><td>u</td><td>o</td>
<td>CJ</td><td>Cl</td><td>CJ</td><td>Cl</td>
<td>man</td><td>man</td><td>man</td><td>man</td>
<td>U</td><td>u</td><td>o</td><td>u</td>
<td>Cl</td><td>CJ</td><td>Cl</td><td>CJ</td>
<td>man</td><td>man</td><td>man</td><td>man</td>
<td>U</td><td>u</td><td>u</td><td>u</td>
<td>CL</td><td>CJ</td><td>Cl</td><td>CJ</td>
<td>man</td><td>man</td><td>man</td><td>man</td>
<td>U</td><td>u</td><td>u</td><td>u</td>
<td>CL</td><td>CJ</td><td>CJ</td><td>Cl</td>
<td>man</td><td>man</td><td>man</td><td>man</td>
<td>U</td><td>u</td><td>u</td><td>o</td>
<td>σ</td><td>o</td><td>ι-H</td><td>CM</td>
<td>Uh</td><td>V</td><td></td><td></td>
<td> •</td><td> •</td><td></td><td> «</td>
<td>M</td><td>M</td><td>m</td><td>hd</td>
Um
n> 1 c
go
• S • H {0 • rd
C
N • rd
G
CM
I m
<img file="LT3295B_D0013.tif" />
fl
G
MG Table
<img file="LT3295B_D0014.tif" />
LO
<td>E</td><td></td><td>H</td><td></td>
<td>rH</td><td></td><td>r *</td><td></td>
<td>K</td><td></td><td>E</td><td></td>
<td>ε</td><td></td><td>rH</td><td></td>
<td>k'— '</td><td></td><td></td><td></td>
<td></td><td></td><td>ε</td><td></td>
<td>CM</td><td></td><td> —</td><td></td>
<td> 00</td><td></td><td>CM</td><td></td>
<td>K</td><td></td><td>CO</td><td></td>
<td>LD</td><td></td><td>l</td><td></td>
<td></td><td></td><td>LO</td><td></td>
<td>χ's,</td><td></td><td>l</td><td>X out</td>
<td>E</td><td></td><td></td><td>E</td>
<td>CM</td><td></td><td>E</td><td>rH</td>
<td></td><td></td><td>CM</td><td>K</td>
<td>G</td><td></td><td>l.</td><td> 3</td>
<td>k— * ·</td><td></td><td>G</td><td></td>
<td></td><td>E</td><td></td><td></td>
<td>co</td><td>rH</td><td>co</td><td>co</td>
<td> 00</td><td>k.</td><td>m</td><td>rH</td>
<td>k.</td><td>ε</td><td>l</td><td></td>
<td></td><td> *—*</td><td>Ν '</td><td>r-</td>
<td></td><td>co</td><td> «.</td><td>k.</td>
<td>s— *.</td><td>rH</td><td></td><td></td>
<td>E</td><td>k.</td><td>E</td><td>X</td>
<td>CM</td><td>r *</td><td>CM</td><td>rH</td>
<td></td><td></td><td>l</td><td></td>
<td>ε</td><td></td><td>ε</td><td> 6</td>
<td>• '—τ</td><td>X</td><td> ·»«*</td><td> ·»—«·</td>
<td>CM</td><td>rH</td><td>Cd</td><td>CO</td>
<td>σ</td><td>Cl</td><td>σ</td><td>σ</td>
<td></td><td>ε</td><td>• i</td><td></td>
<td>m</td><td> *—'</td><td> 00</td><td>LO</td>
CM
I m
(0
C
Φ • G
G
<td colspan="4"></td><td colspan="3"> 00</td>
<td></td><td></td><td></td><td></td><td>1 m</td><td></td><td></td>
<td>co</td><td></td><td>Ν '</td><td></td><td>fl</td><td></td><td>co</td>
<td> 1</td><td></td><td> 1</td><td></td><td> •—1</td><td></td><td>I</td>
<td>co</td><td></td><td>n</td><td></td><td>• G</td><td></td><td>to</td>
<td> (0</td><td></td><td>fl</td><td></td><td>C</td><td></td><td>fl</td>
<td>i-1</td><td></td><td> »—1</td><td></td><td>fl</td><td></td><td> 1—1</td>
<td>-G</td><td></td><td>• G</td><td></td><td>G</td><td></td><td>• G</td>
<td>C</td><td></td><td>C</td><td></td><td>-G</td><td></td><td>C</td>
<td>fl</td><td> 1</td><td> <0</td><td> 1</td><td>Ct</td><td> 1</td><td>fl</td>
<td>G</td><td> -</td><td>G</td><td> »</td><td>υ</td><td> •</td><td>G</td>
<td>-G</td><td> 1</td><td>G</td><td> 1</td><td>-G</td><td> 1</td><td>-G</td>
<td>(X</td><td></td><td>a</td><td></td><td>G</td><td></td><td>Ct</td>
<td>O</td><td></td><td>o</td><td></td><td>O</td><td></td><td> 0</td>
<td>G</td><td></td><td>G</td><td></td><td>G</td><td></td><td>G</td>
<td>Ό</td><td></td><td>n</td><td></td><td>Tl</td><td></td><td>τι</td>
<td>• G</td><td></td><td>G</td><td></td><td>-G</td><td></td><td>• rd</td>
<td>E</td><td></td><td>E</td><td></td><td>E</td><td></td><td>E</td>
<td> (0</td><td></td><td>fl</td><td></td><td>fl</td><td></td><td>fl</td>
<td>G</td><td></td><td>G</td><td></td><td>G</td><td></td><td>G</td>
<td>G</td><td></td><td>G</td><td></td><td>G</td><td></td><td>G</td>
<td>Φ</td><td></td><td>(D</td><td></td><td>Φ</td><td></td><td>Φ</td>
<td>G</td><td></td><td>G</td><td></td><td>G</td><td></td><td>G</td>
<td>to</td><td>to fl rH</td><td>to</td><td>ow] rd rH</td><td>to</td><td>to rH</td><td>to</td><td>CO <d rH</td>
<td>fl</td><td>♦ rd</td><td>fl</td><td>♦ rd</td><td>fl</td><td>• rd</td><td>fl</td><td>• rd</td>
<td>rd</td><td>Ct</td><td>rH</td><td>Ct</td><td>rH</td><td>Ct</td><td>rH</td><td>(i.e.</td>
<td>• rd</td><td> 0</td><td>rd</td><td>o</td><td>• rd</td><td> 0</td><td>• rd</td><td>o</td>
<td>G</td><td>G</td><td>G</td><td>G</td><td>G</td><td>G</td><td>G</td><td>G</td>
<td>Φ</td><td>Ct</td><td>Φ</td><td>Ct</td><td>Φ</td><td>Ct</td><td>Φ</td><td>Ct</td>
<td>rH</td><td>CM</td><td>CO</td><td>Ν '</td><td>E</td><td>LO</td><td>r-</td><td> 00</td>
uo
-P
Zoo
C
O
-H <Ū • H
G • H λ:
• H
N • H
Ml
CM
X!
r — I £
CM x
LO
X
CM
X »—I ε"
X r — I
X _ε
CM
LO
X
CM
X «“ H
X
G co x
LO
X
X ε
£ ro r — j co cn
X kO
X
CM
O
CM
X
CM
X i-I ε
x
CM
O
CM
X
CM
X rH ε
<td> --’</td><td></td><td> —</td><td></td><td> —</td><td></td><td>n</td><td> —</td><td>o</td><td>X— '</td><td>o</td>
<td>co</td><td>co</td><td>co</td><td>co</td><td>CM</td><td></td><td></td><td>kO</td><td>m</td><td>kO</td><td>LO</td>
<td>co</td><td></td><td>co</td><td>t-1</td><td> 00</td><td></td><td></td><td></td><td>X</td><td></td><td>X</td>
<td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td>
<td>X</td><td>x</td><td>X</td><td>X</td><td>K</td><td></td><td>Λ.1</td><td>X</td><td> 00</td><td>X</td><td> 00</td>
<td></td><td>r-</td><td></td><td>Γ-</td><td>kO</td><td></td><td>LN 00</td><td></td><td></td><td></td><td></td>
<td>x</td><td>x</td><td>x</td><td>X</td><td>X</td><td></td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td>
<td></td><td></td><td></td><td>X> X.</td><td></td><td></td><td>kO</td><td></td><td></td><td></td><td></td>
<td>X</td><td>X</td><td>K</td><td>X</td><td>sc</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td>
<td>CM</td><td>r-1</td><td>CM</td><td>iH</td><td>CM</td><td>r-1</td><td>3c</td><td>CM</td><td>r-1</td><td>CM</td><td>r - t</td>
<td>X</td><td>x</td><td>x</td><td></td><td>X</td><td>X</td><td>c3</td><td>X</td><td>X</td><td>X</td><td>X</td>
<td>ε</td><td>ε</td><td>G</td><td>ε</td><td> 4-></td><td>ε</td><td>X</td><td>ε</td><td>ε</td><td>ε</td><td> 3</td>
<td> *«—*</td><td></td><td> ·—</td><td></td><td> ·—*</td><td> ·*—»·</td><td> 4-»</td><td>χ— *</td><td>χ— *</td><td>X- * »</td><td></td>
<td>o</td><td>co</td><td>o</td><td>co</td><td>O</td><td>co</td><td></td><td>O</td><td>r-</td><td>o</td><td>r-</td>
<td>o</td><td>σι</td><td>o</td><td>o></td><td>CO</td><td>T-1</td><td>O co</td><td></td><td>kO</td><td>o</td><td>L0</td>
<td>X</td><td>X.</td><td>X.</td><td>X.</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td>
<td></td><td>kO</td><td></td><td>kO</td><td></td><td>r-</td><td></td><td>co</td><td>r-</td><td></td><td>r-</td>
<td>CM 1</td><td>CM 1</td>
<td> 1</td><td>ra</td>
<td></td><td>ie</td>
<td>r-1</td><td>A</td>
<td>• H</td><td>A</td>
<td></td><td>P</td>
<td>• r4</td><td>• H</td>
<td>P</td><td>H</td>
<td>• H</td><td>A</td>
<td>Ch</td><td>IX</td>
continuation of the table
<td>v 1</td><td colspan="2">co 1</td><td>co 1</td><td>co 1</td><td>CO</td><td>co 1</td>
<td>ra</td><td></td><td>ra</td><td>ra</td><td>ra</td><td> 1</td><td>ra</td>
<td>ie</td><td></td><td>ie</td><td>ie</td><td>ie</td><td>ra</td><td>ie</td>
<td>i-1</td><td></td><td>i-1</td><td>A</td><td>i-1</td><td>ie</td><td>i-1</td>
<td>A</td><td></td><td>A</td><td>A</td><td>A</td><td>i-1</td><td>A</td>
<td>C</td><td></td><td>C</td><td>C</td><td>G</td><td>A</td><td>G</td>
<td>ie</td><td> 1</td><td>ie</td><td>ie</td><td>ie</td><td>G</td><td>ie</td>
<td>it</td><td> -</td><td>M</td><td>M</td><td>M</td><td>ie</td><td>H</td>
<td>A</td><td> 1</td><td>A</td><td>A</td><td>A</td><td>it</td><td>A</td>
<td>oh,</td><td></td><td>X</td><td>X</td><td>X</td><td>A</td><td>X</td>
<td> 0</td><td></td><td> 0</td><td> 0</td><td> 0</td><td>X</td><td> 0</td>
<td>st</td><td></td><td>M</td><td>μ</td><td> +1</td><td> 0</td><td>M</td>
<td>P</td><td></td><td>P</td><td>P</td><td>P</td><td>il</td><td>P</td>
<td>A</td><td></td><td>A</td><td>• H</td><td>A</td><td>P</td><td>• rM</td>
<td>X</td><td></td><td>X</td><td>X</td><td>X</td><td>• rd</td><td>X</td>
<td>ie</td><td></td><td>ie</td><td>ie</td><td>ie</td><td>X</td><td>ie</td>
<td>G</td><td></td><td>M</td><td>n</td><td>M</td><td>ie</td><td>n</td>
<td>A</td><td></td><td>A</td><td>A</td><td>A</td><td>M</td><td>A</td>
<td>d)</td><td></td><td>d)</td><td>d)</td><td>d)</td><td>d)</td><td>d)</td>
<td>A</td><td></td><td>A</td><td>A</td><td>A</td><td>A</td><td>A</td>
<td></td><td>ra</td><td></td><td>ra</td><td></td><td>ra</td><td></td><td>M</td>
<td></td><td>ie</td><td></td><td>ie</td><td></td><td>ie</td><td></td><td>ie</td>
<td>ω</td><td>i-t</td><td>ra</td><td>i-4</td><td></td><td> 1—1</td><td>ra</td><td>A</td>
<td><ϋ</td><td>A</td><td>ie</td><td>• rd</td><td><U</td><td>A</td><td>ie</td><td>A</td>
<td>t-1</td><td>X</td><td>A</td><td>X</td><td>rH</td><td>X</td><td>i-t</td><td>X</td>
<td>• H</td><td> 0</td><td>A</td><td> 0</td><td>• H</td><td>o</td><td>A</td><td> 0</td>
<td>4J</td><td>Jl</td><td>A</td><td>M</td><td>-U</td><td>K</td><td>A</td><td>M</td>
<td></td><td>X</td><td>d)</td><td>X</td><td> 0)</td><td>X</td><td>d)</td><td>X</td>
CM
<td></td><td>O</td><td>rl</td><td>CM</td><td>CO</td><td>V</td><td>LO</td><td>kO</td>
<td>σ</td><td>t-4</td><td></td><td>r-4</td><td>t 't</td><td>t<sup>-</sup>1</td><td> <-4</td><td> »—1</td>
<td>CM</td><td>CM</td><td>CM</td><td>CM</td><td>CM</td><td>CM</td><td>CM</td><td>CM</td>
.17 ethyl tetrahydrothiopyranyl-3--4.46 (t, 2H), 7.20 (m, 2H), 7.67 (1H), 8.50 (m, 1H)
CM cP
J
N
Μ4 se
<td colspan="3">Uh Uh k r-</td><td colspan="3">m cn k r-</td><td colspan="2">k</td><td></td>
<td>k</td><td> *»</td><td></td><td>k.</td><td></td><td></td><td></td><td>K</td><td> 35</td>
<td> 35</td><td>B</td><td> 35</td><td> 35</td><td></td><td></td><td></td><td>tH</td><td>tH</td>
<td>CM</td><td>rH k</td><td>CM</td><td>rH</td><td></td><td></td><td></td><td>e</td><td>k £</td>
<td>4J</td><td>This one</td><td>4J</td><td> £</td><td></td><td></td><td></td><td></td><td></td>
<td>«—X</td><td></td><td></td><td></td><td></td><td></td><td></td><td>o</td><td>co</td>
<td>o</td><td>co</td><td>o</td><td>co</td><td></td><td></td><td></td><td>o</td><td>CO</td>
<td>rH</td><td>CM</td><td>rH</td><td>CM</td><td></td><td></td><td></td><td>k</td><td>k</td>
<td>k</td><td>k</td><td>k</td><td>k</td><td></td><td></td><td></td><td>LO</td><td>r *</td>
<td>M *</td><td>LO</td><td></td><td>co</td><td></td><td></td><td></td><td></td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>k</td><td>k</td>
<td>k</td><td>k</td><td>k</td><td>k</td><td></td><td></td><td></td><td></td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>Ή</td><td>T *</td>
<td>X</td><td> 35</td><td> 35</td><td> 35</td><td></td><td></td><td></td><td>U U CM</td><td>U- | rH</td>
<td>CM</td><td>, H</td><td>CM</td><td>«Η</td><td></td><td></td><td></td><td></td><td></td>
<td>k 3</td><td>k Come on</td><td>k £.</td><td>k £.</td><td>CM</td><td>CM</td><td> 00</td><td>-P</td><td> 3</td>
<td>co</td><td>o</td><td><n</td><td>o</td><td> 00</td><td>LD</td><td>tn</td><td>O</td><td>co</td>
<td>CT)</td><td>o</td><td>σ</td><td>o</td><td> 1</td><td> 1</td><td> 1</td><td>rH</td><td>CM</td>
<td></td><td></td><td>k</td><td></td><td> 00</td><td> 00</td><td>'T</td><td>k.</td><td>k</td>
<td>m</td><td>LO</td><td>m</td><td>LO</td><td>r-</td><td>v</td><td>m</td><td></td><td>co</td>
mu
Γ — 1
H tl thienyl-2 Table 72-74 ° 4C aio νχΖ'ζ
X
I tM
<td colspan="2"></td><td colspan="5">Uh 1 to</td>
<td>Uh</td><td></td><td></td><td></td><td> <0</td><td></td><td></td>
<td> 1</td><td></td><td> 1</td><td></td><td>i-1</td><td></td><td></td>
<td>m</td><td></td><td>n</td><td></td><td>-H</td><td></td><td></td>
<td> (0</td><td></td><td> (0</td><td></td><td>C</td><td></td><td></td>
<td>i-1</td><td></td><td>i-1</td><td></td><td> !3</td><td></td><td></td>
<td>H</td><td></td><td>• rH</td><td></td><td>tl</td><td></td><td></td>
<td>C</td><td></td><td>C</td><td></td><td>• H</td><td></td><td></td>
<td>u</td><td> 1</td><td></td><td> 1</td><td>a</td><td> 1</td><td>I</td>
<td>tl</td><td> -</td><td>tl</td><td> -</td><td> 0</td><td> -</td><td> -</td>
<td>• H</td><td>Ί</td><td>• r4</td><td>Ί</td><td>• H</td><td> 1</td><td> 1</td>
<td>d</td><td></td><td>d</td><td></td><td>4J</td><td></td><td></td>
<td> 0</td><td></td><td> 0</td><td></td><td>O</td><td></td><td></td>
<td>tl</td><td></td><td>tl</td><td></td><td>tl</td><td></td><td></td>
<td>τ)</td><td></td><td>'D</td><td></td><td>T5</td><td></td><td></td>
<td>• H</td><td></td><td>-H</td><td></td><td>Ή</td><td></td><td></td>
<td>n</td><td></td><td>Λ</td><td></td><td>Λ</td><td></td><td></td>
<td> <0</td><td></td><td>(U</td><td></td><td>Φ</td><td></td><td></td>
<td>tl</td><td></td><td>tl</td><td></td><td>tl</td><td></td><td></td>
<td> 4-1</td><td></td><td>4</td><td></td><td> 4-1</td><td></td><td></td>
<td>Φ</td><td></td><td>d)</td><td></td><td>Φ</td><td></td><td></td>
<td>4</td><td></td><td> 4-1</td><td></td><td> 4-1</td><td></td><td></td>
<td></td><td> <0</td><td></td><td>n</td><td></td><td> 0)</td><td></td>
<td></td><td> (0</td><td></td><td>u</td><td></td><td>Φ</td><td></td>
<td>n</td><td>r-1</td><td>M</td><td>i-1</td><td> 03</td><td>rH</td><td> 0)</td>
<td>(U</td><td>-H</td><td> (0</td><td>• H</td><td>Φ</td><td>Ή</td><td>Φ</td>
<td>i-1</td><td>d</td><td>i-1</td><td>a</td><td> '—1</td><td>a</td><td>f-1</td>
<td>• H</td><td>O</td><td>• r4</td><td>o</td><td>-H</td><td>o</td><td>• H</td>
<td>4</td><td>tl</td><td>4</td><td>tl</td><td>-Ut</td><td> 14</td><td> 4-1</td>
<td>Φ</td><td>d</td><td>Φ</td><td>a</td><td>Φ</td><td>a</td><td>Φ</td>
cn csl
C £
I-I
<td>iH</td><td>CM</td><td>co</td><td></td><td>m</td><td>LO</td><td>r *</td>
<td>CO</td><td>CO</td><td>co</td><td>co</td><td>Uh</td><td>CO</td><td>co</td>
X
τ) ė
m ro
X f
<td> *»</td><td>X</td><td colspan="3">X</td><td colspan="4">X</td><td colspan="4">X</td>
<td>^ -χ »</td><td></td><td></td><td></td><td></td><td></td><td>X—</td><td></td><td></td><td>x</td><td></td><td></td><td></td>
<td>s</td><td>S</td><td></td><td></td><td>X</td><td>X</td><td>X</td><td>K</td><td></td><td>X</td><td></td><td></td><td></td>
<td>CM</td><td>rH</td><td></td><td></td><td>rH</td><td>rH</td><td>rH</td><td>rH</td><td></td><td>CM</td><td></td><td></td><td></td>
<td></td><td>x</td><td></td><td></td><td>x</td><td>X</td><td>x</td><td>X</td><td></td><td>X</td><td></td><td></td><td></td>
<td> 4-1</td><td>ε</td><td></td><td></td><td>ε</td><td>ε</td><td>ε</td><td>ε</td><td></td><td>ε</td><td></td><td></td><td></td>
<td>* —R</td><td></td><td></td><td></td><td></td><td> ·*-*·</td><td> *«—*</td><td></td><td></td><td>X—-</td><td></td><td></td><td></td>
<td>o</td><td>co</td><td></td><td></td><td>CM</td><td>co</td><td>CM</td><td>m</td><td></td><td>LO</td><td></td><td></td><td></td>
<td>rH</td><td>στ</td><td></td><td></td><td>co</td><td>rH</td><td> 00</td><td>rH</td><td></td><td>σι</td><td></td><td></td><td></td>
<td> »„</td><td>x</td><td></td><td></td><td>X</td><td>χ</td><td>X</td><td>X</td><td></td><td>X</td><td></td><td></td><td></td>
<td></td><td>kO</td><td></td><td></td><td>LO</td><td>r-</td><td>kO</td><td>r-</td><td></td><td>LO</td><td></td><td></td><td></td>
<td>x</td><td>x</td><td></td><td></td><td>X</td><td>x</td><td>X</td><td>X</td><td></td><td>X</td><td>X</td><td></td><td></td>
<td></td><td></td><td></td><td></td><td></td><td>, ^ - χ</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td>
<td>E</td><td></td><td></td><td></td><td>X</td><td>X</td><td>X</td><td>X</td><td></td><td>X</td><td>X</td><td></td><td></td>
<td>CM</td><td>rH</td><td></td><td></td><td>CM</td><td>rH</td><td>CM</td><td>rH</td><td></td><td>CM</td><td>rH</td><td></td><td></td>
<td>x</td><td>x</td><td></td><td></td><td>X</td><td>χ</td><td>X</td><td>X</td><td></td><td>X</td><td>X</td><td>r-</td><td></td>
<td>ε</td><td>Come on</td><td></td><td></td><td>-P</td><td>ε</td><td>P</td><td> 3</td><td></td><td> 4-»</td><td> 3</td><td>o</td><td></td>
<td> ·*—'</td><td></td><td>o</td><td> 00</td><td> --,</td><td></td><td>'M- *'</td><td></td><td>sr</td><td> ’*-*</td><td></td><td>rH</td><td>o</td>
<td>CO</td><td>CM</td><td>σι</td><td>m</td><td>CM</td><td>co</td><td>CM</td><td>m</td><td>r-</td><td>U0</td><td>m</td><td> 1</td><td>r-</td>
<td>στ</td><td> 00</td><td> 1</td><td> 1</td><td>rH</td><td>στ</td><td>rH</td><td>σι</td><td> 1</td><td>O</td><td>CM</td><td>LD</td><td> 1</td>
<td>x</td><td> «.</td><td>LO</td><td>m</td><td>x</td><td>x</td><td>x</td><td>X</td><td>ro</td><td>X</td><td>X</td><td>o</td><td> 00</td>
<td>co</td><td>kO</td><td> 00</td><td>LD</td><td></td><td>kO</td><td></td><td>L0</td><td></td><td>• r</td><td>r ·</td><td>rH</td><td>LO</td>
<img file="LT3295B_D0015.tif" />
<td>ro I</td><td>S</td><td>ro I</td>
<td>1 to</td><td> 1</td><td>1 W</td>
<td> (0</td><td></td><td>(U</td>
<td> <—1</td><td></td><td> »—1</td>
<td>G</td><td></td><td>G</td>
<td>C</td><td></td><td>G</td>
<td>Φ</td><td></td><td>Φ</td>
<td>• G</td><td></td><td>• G</td>
<td> 4-></td><td></td><td>P</td>
et table continuation m
in
<td colspan="2"> 1</td><td colspan="2"><TJ rp</td><td colspan="2">ro l</td><td>v 1</td>
<td>to</td><td></td><td>P</td><td></td><td>to</td><td></td><td>to</td>
<td>(tj</td><td></td><td>c</td><td></td><td>(tJ</td><td></td><td>lu</td>
<td>rH</td><td></td><td>Π3</td><td></td><td>x</td><td></td><td>X</td>
<td>H</td><td></td><td>G</td><td></td><td>• G</td><td></td><td>• G</td>
<td>c</td><td></td><td>-P</td><td></td><td>G</td><td></td><td>C</td>
<td>(tj</td><td> 1</td><td>£ h</td><td> 1</td><td>f3</td><td> 1</td><td> <3</td>
<td>M • P</td><td>Ί</td><td>0 • P</td><td> =</td><td>G • G</td><td>Ί</td><td>G -G</td>
<td>oh,</td><td></td><td>X</td><td></td><td>a</td><td></td><td>Ih</td>
<td>o</td><td></td><td> 0</td><td></td><td>o</td><td></td><td>O</td>
<td>G</td><td></td><td>G</td><td></td><td>G</td><td></td><td>G</td>
<td>Tl</td><td></td><td>Tl</td><td></td><td>Tl</td><td></td><td>T3</td>
<td>• P</td><td></td><td>• P</td><td></td><td>• G</td><td></td><td>• G</td>
<td>X</td><td></td><td>X</td><td></td><td>X</td><td></td><td>X</td>
<td>(ow</td><td></td><td>(U</td><td></td><td> (0</td><td></td><td> <3</td>
<td>G</td><td></td><td>G</td><td></td><td>G</td><td></td><td>G</td>
<td>X</td><td></td><td>X</td><td></td><td>X</td><td></td><td>X</td>
<td>d)</td><td></td><td>Φ</td><td></td><td>Φ</td><td></td><td>Φ</td>
<td> 4-1</td><td></td><td>X</td><td></td><td>X</td><td></td><td>X</td>
<td>to</td><td colspan="3">to</td><td> (0</td><td colspan="2">to</td><td colspan="2">to</td>
<td> (0</td><td></td><td></td><td></td><td> <0</td><td></td><td>al</td><td></td><td></td>
<td>rp</td><td>to</td><td> »-1</td><td>to</td><td>X</td><td>ca</td><td>ip</td><td>m</td><td> 1—1</td>
<td>P</td><td>rfl</td><td>-G</td><td> (0</td><td>• G</td><td>aj</td><td>• P</td><td> (0</td><td>• G</td>
<td>(h</td><td> <—1</td><td>a</td><td>rp</td><td>Ih</td><td>rp</td><td>a</td><td>X</td><td>ih</td>
<td>o</td><td>G</td><td>o</td><td>• P</td><td>o</td><td>-P</td><td>o</td><td>-G</td><td>X</td>
<td>G</td><td>X</td><td>G</td><td>X</td><td>G</td><td>-P</td><td>P</td><td>X</td><td>o</td>
<td>Ih</td><td>Φ</td><td>Ih</td><td>Φ</td><td>Ih</td><td>Φ</td><td>a</td><td>Φ</td><td>CU</td>
<td></td><td></td><td>o</td><td>rH</td><td>CM</td><td>CO</td><td></td><td>m</td><td>LO</td>
<td> 00</td><td>σι</td><td>rH</td><td>rH</td><td>rH</td><td>rp</td><td>rH</td><td>I-1</td><td>I-1</td>
.17 Ethyl Tetrahydrothiopyranyl-3 - 57-59
<td>X i-1</td><td>X i-1</td><td>X rd</td><td>X 1-1</td>
<td></td><td>he.</td><td></td><td></td>
<td>E.</td><td>E</td><td>E</td><td>E</td>
<td></td><td>> —R</td><td>• r</td><td></td>
<td>X</td><td>X</td><td>X</td><td>X</td>
<td>X</td><td>X</td><td>X</td><td>X</td>
<td>K</td><td>he.</td><td></td><td></td>
<td>kO</td><td>MO</td><td>MO</td><td>kO</td>
<td>X</td><td>he.</td><td></td><td> ·*</td><td></td><td> *</td><td>he.</td><td>he.</td><td>he.</td><td>X</td><td>X</td>
<td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>t 'd</td><td>i-d</td>
<td>he. E</td><td>X he.</td><td>r-1 K</td><td>X</td><td>i-l he.</td><td>X</td><td>r-1</td><td>X <</td><td>id he.</td><td>E</td><td>e</td>
<td></td><td>-P</td><td>Come on</td><td>P</td><td>E,</td><td> 4-></td><td>E</td><td>-P</td><td>, ε</td><td></td><td></td>
<td rowspan="2">s-</td><td></td><td></td><td></td><td></td><td> *—*·</td><td></td><td></td><td></td><td>o</td><td>co</td>
<td>CM</td><td>MO</td><td>X</td><td>MO</td><td>X</td><td>MO</td><td>X</td><td>MO</td><td>σ »</td><td>LO</td>
<td>he.</td><td>i-l</td><td>O</td><td>i-l</td><td>O</td><td>i-l</td><td>O</td><td>rd</td><td>O</td><td></td><td></td>
<td>MO</td><td>K</td><td></td><td></td><td>V</td><td>k</td><td></td><td></td><td></td><td>m</td><td>kO</td>
<td></td><td>sr</td><td>kO</td><td></td><td>kO</td><td></td><td>kO</td><td></td><td>MO</td><td></td><td></td>
<td>he. K</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td>
<td></td><td>he.</td><td> *·</td><td></td><td>K</td><td></td><td> *·</td><td></td><td>he.</td><td></td><td>X—.</td>
X
I "I ta.
ε
X i-I
E
X r - l,
E rc x
r - l
E rc x
K i-l
E
X
T — I ta.
E
<td></td><td>m</td><td>X</td><td>o</td><td>o</td><td>o</td><td>o</td><td>o</td><td>o</td><td>o</td><td>o</td><td>X</td><td>kO</td>
<td>N</td><td>o</td><td>X</td><td><Tj</td><td>σ></td><td>(Ti</td><td>σι</td><td>o</td><td>σι</td><td>o</td><td>σι</td><td> 1—1</td><td>O</td>
<td>; P</td><td></td><td>he.</td><td></td><td></td><td></td><td>he.</td><td></td><td>K</td><td>he.</td><td>v</td><td></td><td> *.</td>
<td> 4-4</td><td></td><td>r *</td><td>X</td><td>X</td><td>ro</td><td>X</td><td></td><td>LO</td><td></td><td>X</td><td>-r</td><td>kO</td>
xi
nm
x
I m
(Oops
8*
p. · —I • H -P g
op
• H
P, ι — I • HP
<td>X I</td><td>I</td><td>CO |</td>
<td>1 CO</td><td>1 CO</td><td>co</td>
<td> <0</td><td></td><td>fU</td>
<td>t-1</td><td>r - l</td><td>r - l</td>
<td>• H</td><td>• rd</td><td>• rd</td>
table continuation ct
P • H
Cu o
• H
Cl
4-1
0)
4J
Cl
Ή p, o
• H no
4->
Φ
4-)
P
P &
• rd
P
4->
Φ
P
<td>to</td><td></td><td>to</td><td></td><td></td><td></td>
<td> (0</td><td></td><td> (0</td><td></td><td></td><td></td>
<td>I<sup>-</sup>1</td><td>to</td><td>i-d</td><td>to</td><td>to</td><td>to</td>
<td>• rd</td><td>lt)</td><td>• rd</td><td>lt)</td><td>n)</td><td>lt)</td>
<td> 0,</td><td>i-1</td><td> 0.</td><td>r<sup>-</sup>1</td><td>i-1</td><td> <—1</td>
<td>o</td><td>-P</td><td> 0</td><td>-P</td><td>• P</td><td>-P</td>
<td>P</td><td>X</td><td>P</td><td> 4-1</td><td> 4-1</td><td> 4-4</td>
<td>P.</td><td>Φ</td><td>P.</td><td>Φ</td><td>Φ</td><td>Φ</td>
<td>co</td><td>σι</td><td>o</td><td>Tp</td><td>X</td><td>X</td>
<td>i-1</td><td>τΡ</td><td>X</td><td>X</td><td>X</td><td>X</td>
<td>CO</td><td>X</td><td>X</td><td>X</td><td>X</td><td>x '</td>
3.24 propyl tetrahydropyraryl-3'-methylpyrrolyl-2 4.12 (t, 2H), 5.90 (m, 1H),
6.06 (m, 1H), 6.53 (m, 1H)
X nD-CH<sub>2</sub>CHC ^ 2 ~ ©
Xo
U o
p *> 1
C <0 • rd
C i
• H
N • H
Ml • Φ
Φ
-P c
Φ
<img file="LT3295B_D0016.tif" />
ch4
CL
X i
co
IIs
os
<td colspan="2">X co</td><td colspan="2">E n</td><td>E cn</td><td>E m</td><td colspan="3">E n</td>
<td></td><td></td><td></td><td></td><td></td><td> *.</td><td></td><td> *.</td><td></td>
<td></td><td>ε</td><td></td><td>ε</td><td>ε</td><td>ε</td><td></td><td>ε.</td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td>
<td></td><td>o</td><td></td><td>o</td><td>o</td><td>o</td><td></td><td>o</td><td></td>
<td></td><td>CN</td><td></td><td>CN</td><td>CM</td><td>CM</td><td></td><td>n</td><td></td>
<td></td><td> *»</td><td></td><td>Q.</td><td></td><td>κ</td><td></td><td>K,</td><td></td>
<td></td><td>r ~~ 1</td><td>i-1</td><td>r- 1</td><td>r- 1</td><td>Γ 1</td><td>o</td><td>r- 1</td><td>o</td>
<td></td><td>tn</td><td>CO</td><td>o</td><td>o</td><td>o</td><td>• r</td><td>o</td><td>co</td>
<td></td><td> 00</td><td> 1</td><td></td><td>r-</td><td>r-</td><td> 1</td><td> 00</td><td> 1</td>
<td>m</td><td></td><td>Ch</td><td>K</td><td></td><td></td><td> 00</td><td>K</td><td> 00</td>
<td>n</td><td>co</td><td>tn</td><td>co</td><td>co</td><td>co</td><td>n</td><td>co</td><td>tn</td>
<td>CM |</td><td> 1</td><td> 1</td><td> 1</td><td> 1</td><td> 1</td><td>n 1</td><td> 1</td><td>CO |</td>
<td>f C0</td><td>Ί</td><td>Ί</td><td>Ί</td><td>Ί</td><td>Ί</td><td>1 tn</td><td> =.</td><td>1 CO</td>
<td> <0</td><td></td><td></td><td></td><td></td><td></td><td><d</td><td></td><td></td>
<td><"D</td><td></td><td></td><td></td><td></td><td></td><td>E</td><td></td><td>r-1</td>
<td>Ή</td><td></td><td></td><td></td><td></td><td></td><td>• P</td><td></td><td>• r4</td>
<td>C</td><td></td><td></td><td></td><td></td><td></td><td>C</td><td></td><td>a</td>
<td>Φ</td><td></td><td></td><td></td><td></td><td></td><td>Φ</td><td></td><td>φ</td>
<td>Ή</td><td></td><td></td><td></td><td></td><td></td><td>• H</td><td></td><td>• H</td>
<td>P</td><td></td><td></td><td></td><td></td><td></td><td>E</td><td></td><td>P</td>
ni
m
<td colspan="2">cn 1</td><td colspan="2"> 1</td><td colspan="2">ra P</td><td colspan="2">cn 1</td><td> 1</td>
<td>tn</td><td></td><td>m</td><td></td><td>Ή</td><td></td><td>n</td><td></td><td>Oops</td>
<td>td</td><td></td><td>(d</td><td></td><td>c</td><td></td><td>(d</td><td></td><td>(d</td>
<td>p - t</td><td></td><td>> —I</td><td></td><td>id</td><td></td><td> »—1</td><td></td><td>E</td>
<td>P</td><td></td><td>P</td><td></td><td>P</td><td></td><td>• P</td><td></td><td>• P</td>
<td>C</td><td></td><td>c</td><td></td><td>• H</td><td></td><td>C</td><td></td><td>c</td>
<td><d</td><td> 1</td><td>fd</td><td> 1</td><td>a</td><td> 1</td><td>(d</td><td> 1</td><td>J3</td>
<td>P • P</td><td>Ί</td><td>P • P</td><td>Ί</td><td>o • P</td><td>Ί</td><td>P -P</td><td>Ί</td><td>P -P</td>
<td>a</td><td></td><td>a</td><td></td><td>E</td><td></td><td> 0.</td><td></td><td>a</td>
<td>o</td><td></td><td> 0</td><td></td><td>O</td><td></td><td>O</td><td></td><td> 0</td>
<td>P</td><td></td><td>P</td><td></td><td>P</td><td></td><td>P</td><td></td><td>P</td>
<td>Ό</td><td></td><td>TJ</td><td></td><td> 9</td><td></td><td>T!</td><td></td><td>E</td>
<td>• H E</td><td></td><td>Ή E</td><td></td><td>-P E</td><td></td><td>Ή E</td><td></td><td>• P E</td>
<td>(d P</td><td></td><td><3 P</td><td></td><td>f3 P</td><td></td><td>(3 P</td><td></td><td>(3 P</td>
<td>-P</td><td></td><td> 4-4</td><td></td><td>E</td><td></td><td>E</td><td></td><td>E</td>
<td>Φ</td><td></td><td>Φ</td><td></td><td>Φ</td><td></td><td>Φ</td><td></td><td>Φ</td>
<td> 4-1</td><td></td><td>-P</td><td></td><td>E</td><td></td><td>E</td><td></td><td>E</td>
<td>co</td><td>tn (d i-1</td><td>w</td><td>to {di — I</td><td>CO</td><td>tn (d E</td><td>co</td><td>tn td E</td><td>w</td>
<td>ra</td><td>• P</td><td>ra</td><td>-P</td><td>ra</td><td>-P</td><td><a</td><td>• P</td><td>ra</td>
<td><P</td><td>a</td><td>i-1</td><td>Ά</td><td> <—1</td><td>a</td><td>r— |</td><td>a</td><td> 1—1</td>
<td>• rd</td><td>o</td><td>-H</td><td> 0</td><td>• H</td><td>o</td><td>• H</td><td>o</td><td>• H</td>
<td>p</td><td>P</td><td>P</td><td>P</td><td>-P</td><td>P</td><td>P</td><td>P</td><td>P</td>
<td>Φ</td><td>a</td><td>Φ</td><td>a</td><td>Φ</td><td>a</td><td>Φ</td><td>a</td><td>Φ</td>
<td>iH</td><td>CN</td><td>cn</td><td></td><td>LO</td><td>co</td><td>r-</td><td> 00</td><td>Ch</td>
<td>o</td><td>O</td><td>O</td><td>o</td><td>O</td><td>o</td><td>o</td><td>o</td><td>o</td>
M
<td></td><td>B i “H</td><td>a r-1</td><td></td><td>a CN</td><td>a CN</td><td>a CN</td><td>a CN</td><td></td>
<td></td><td></td><td></td><td></td><td>fe.</td><td>fe.</td><td></td><td></td><td></td>
<td></td><td>ε.</td><td> 3</td><td></td><td>ra</td><td>n</td><td>co</td><td>n</td><td></td>
<td></td><td></td><td></td><td></td><td></td><td> *-··*</td><td> *-*'</td><td></td><td></td>
<td></td><td>m</td><td>o</td><td></td><td>lf)</td><td>lf)</td><td>lf)</td><td>m</td><td></td>
<td>χ-fe.</td><td>CN</td><td>n</td><td></td><td>lf)</td><td>Lf)</td><td>lf)</td><td>r *</td><td></td>
<td>3C</td><td></td><td>fe.</td><td></td><td></td><td>fe.</td><td></td><td></td><td></td>
<td>CO</td><td>r-</td><td>r *</td><td></td><td>kO</td><td>kO</td><td>NO</td><td>kO</td><td></td>
<td>fe.</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td>
<td>ε</td><td>fe.</td><td></td><td></td><td></td><td></td><td>fe.</td><td>K</td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td>^ -fe.</td><td>^ -fe.</td><td></td>
<td>o</td><td>al</td><td>a</td><td></td><td>a</td><td>a</td><td>a</td><td>a</td><td></td>
<td>'ShT</td><td>CN</td><td>CN</td><td></td><td>n</td><td>m</td><td>n</td><td>CO</td><td></td>
<td>fe.</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td>
<td>r *</td><td> 3</td><td>e_</td><td></td><td>ra</td><td>co</td><td>co</td><td>co</td><td></td>
<td>I</td><td></td><td></td><td>o</td><td> *—*</td><td>fe *</td><td>> —R</td><td>fe * · '</td><td> 00</td>
<td>o</td><td>o</td><td>o</td><td>lf)</td><td>o</td><td>o</td><td>O</td><td>LO</td><td>lf)</td>
<td> 00</td><td>o</td><td>O)</td><td> 1</td><td></td><td></td><td></td><td> *5*</td><td> 1</td>
<td>fe.</td><td></td><td></td><td> 00</td><td>v,</td><td>fe.</td><td></td><td></td><td>kO</td>
<td>kO</td><td>kO</td><td>^ o</td><td>Ά</td><td>CM</td><td>CM</td><td>CN</td><td>CN</td><td>m</td>
<td></td><td></td><td></td><td>CN I</td><td>CM I</td><td></td><td></td><td></td><td></td>
<td></td><td></td><td></td><td>1 CO</td><td>co</td><td></td><td></td><td></td><td></td>
<td></td><td></td><td></td><td>Π3</td><td> /0</td><td></td><td></td><td></td><td></td>
<td></td><td></td><td></td><td>rH</td><td>rp</td><td></td><td></td><td></td><td></td>
<td></td><td></td><td></td><td>• H</td><td>• H</td><td></td><td></td><td></td><td></td>
<td></td><td></td><td></td><td>C</td><td>C</td><td></td><td></td><td></td><td></td>
<td> 1</td><td> 1</td><td> 1</td><td>Φ</td><td>Φ</td><td> 1</td><td> 1</td><td> 1</td><td> 1</td>
<td>s</td><td> 5</td><td>s</td><td>• rH</td><td>• P</td><td>E</td><td>s</td><td></td><td>S</td>
<td> 1</td><td> 1</td><td> 1</td><td>-P</td><td>-P</td><td> 1</td><td>t</td><td>I</td><td> 1</td>
<td></td><td></td><td></td><td>rH</td><td>rp</td><td></td><td></td><td></td><td></td>
<td></td><td></td><td></td><td>• P</td><td>• P</td><td></td><td></td><td></td><td></td>
<td></td><td></td><td></td><td>-P</td><td>P</td><td></td><td></td><td></td><td></td>
I
Lf)
I
LT) ra> 1
C • H ra {D · a
ra • Φ r — I
Φ a
c
Φ ra ra
H • H b
O
P a
ni
ra n
i do
<td>ra</td><td></td><td>co</td><td>co</td><td>ST</td><td></td><td>ra</td>
<td> 1</td><td></td><td> 1</td><td> 1</td><td> 1</td><td></td><td>rp</td>
<td>P</td><td></td><td>ra</td><td>m</td><td>ra</td><td></td><td>• P</td>
<td>c</td><td></td><td>ra</td><td>ra</td><td>ra</td><td></td><td>S</td>
<td>ra</td><td></td><td>rp</td><td>rp</td><td>rp</td><td></td><td>ra</td>
<td>p</td><td></td><td>• P</td><td>-P</td><td>• P</td><td></td><td>P</td>
<td>p</td><td></td><td>r- · t-.</td><td>c</td><td>c</td><td></td><td>P</td>
<td>a</td><td> 1</td><td> <3</td><td>ra</td><td> <3</td><td> 1</td><td>a</td>
<td>0 • P</td><td>Ί</td><td>P • P</td><td>P • P</td><td>P • P</td><td>ή</td><td>o • rH</td>
<td>P</td><td></td><td>a</td><td>a</td><td>a</td><td></td><td>a</td>
<td>o</td><td></td><td> 0</td><td>o</td><td>o</td><td></td><td>o</td>
<td>P</td><td></td><td>P</td><td>P</td><td>P</td><td></td><td>P</td>
<td>n</td><td></td><td>Ό</td><td>Ό</td><td>n</td><td></td><td>Ό</td>
<td>P</td><td></td><td>• P</td><td>P</td><td>P</td><td></td><td>• P</td>
<td>a</td><td></td><td>a</td><td>a</td><td>a</td><td></td><td>a</td>
<td> <3</td><td></td><td>ra</td><td>ra</td><td>ra</td><td></td><td>ra</td>
<td>P</td><td></td><td>P</td><td>P</td><td>P</td><td></td><td>P</td>
<td>P</td><td></td><td>+ J</td><td>pi</td><td>P</td><td></td><td>a</td>
<td>Φ</td><td></td><td>φ</td><td>φ</td><td>φ</td><td></td><td>φ</td>
<td>-P</td><td></td><td>o</td><td>p)</td><td>P</td><td></td><td>a</td>
<td></td><td>ra</td><td></td><td>ra</td><td></td><td>ra</td><td></td>
w rd I — I Ή 4-J d) rH
-H
Λ
O &
W
Φ rH • <H
-U
0) • H &
&
ra ra
-P
Φ a
o
P a
ra ra r “HH -P Φ
-P
0)
CM co
M * 1 - Vol
Ά in rr «i» - {i oo r «i
M *
T
M * ar m
> 1 c
o
Ή • H
Ή
C • H
N
Ή
X ti
<td>fe</td><td></td><td></td><td></td><td> ,«^</td><td> «^,</td><td></td><td></td><td></td><td></td>
<td>X</td><td>X</td><td></td><td>X</td><td>X</td><td>Χί</td><td></td><td></td><td></td><td></td>
<td>rH</td><td>rH</td><td></td><td>rH</td><td>rH</td><td>rH</td><td></td><td></td><td></td><td></td>
<td></td><td></td><td></td><td>fe</td><td>fe</td><td>fe</td><td>fe</td><td></td><td>fe</td><td></td>
<td>co</td><td>cn</td><td></td><td>co</td><td>ω</td><td>CO</td><td>«-Fe</td><td></td><td>«-Fe</td><td></td>
<td> -—*</td><td></td><td></td><td>fe- *</td><td>fe- *</td><td>fe- *</td><td>X</td><td></td><td>X</td><td></td>
<td>o</td><td>o</td><td></td><td>o</td><td>o</td><td>o</td><td>rH</td><td></td><td>t ~ H</td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td>fe</td><td></td><td></td><td></td>
<td>κ</td><td></td><td></td><td>fe</td><td>fe</td><td>fe</td><td>Ό</td><td></td><td>T></td><td></td>
<td>r-</td><td>r-</td><td></td><td>r-</td><td>r-</td><td>r-</td><td>fe- *</td><td></td><td>Fri— *</td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td>o</td><td></td><td>o</td><td></td>
<td>fe</td><td>fe</td><td></td><td>fe</td><td></td><td>fe</td><td>r-</td><td></td><td></td><td></td>
<td>«—Fe</td><td>«—Fe</td><td></td><td>«—Fe</td><td> «—««</td><td>«—Fe</td><td>fe</td><td></td><td>fe</td><td></td>
<td>X</td><td>E</td><td></td><td>X</td><td>X</td><td>X</td><td>LO</td><td></td><td>vo</td><td></td>
<td></td><td>'T</td><td></td><td>V</td><td>ST</td><td>• T</td><td></td><td></td><td></td><td></td>
<td>fe</td><td>fe</td><td></td><td>fe</td><td>fe</td><td>fe</td><td>fe</td><td></td><td>fe</td><td></td>
<td>ε</td><td>ε</td><td></td><td> 3</td><td>e.</td><td>ε</td><td>«—Fe</td><td></td><td>«-Fe</td><td></td>
<td></td><td>'fe-'</td><td></td><td></td><td></td><td></td><td>X</td><td></td><td>X</td><td></td>
<td>o</td><td>o</td><td></td><td>o</td><td>o</td><td>o</td><td>rH</td><td></td><td>rH</td><td></td>
<td>LO</td><td>LO</td><td></td><td>LO</td><td>LO</td><td>vo</td><td>fe</td><td></td><td>fe</td><td></td>
<td>κ</td><td>Q.</td><td></td><td>fe</td><td>fe</td><td>fe</td><td>X</td><td></td><td>4J</td><td></td>
<td>LO</td><td>LO</td><td></td><td>LO</td><td>vo</td><td>vo</td><td>Ό</td><td></td><td>Ό</td><td></td>
<td> 1</td><td></td><td></td><td></td><td></td><td></td><td>fe- *</td><td></td><td> *—*</td><td></td>
<td>O</td><td>O</td><td></td><td>O</td><td>o</td><td>o</td><td>o</td><td></td><td>o</td><td></td>
<td>rH</td><td>O</td><td></td><td>rH</td><td>rH</td><td>rH</td><td>o</td><td></td><td>o</td><td></td>
<td> *»</td><td>fe</td><td></td><td>fe</td><td>fe</td><td>fe</td><td>fe</td><td></td><td>fe</td><td></td>
<td>LO</td><td>LO</td><td></td><td>LO</td><td>vo</td><td>VO</td><td>LO</td><td></td><td>LO</td><td></td>
<td>fe</td><td>fe</td><td></td><td>fe</td><td>fe</td><td>fe</td><td></td><td></td><td>fe</td><td></td>
<td>«—X</td><td> «-></td><td></td><td>«—Fe</td><td>«—Fe</td><td>«—Fe</td><td>«—Fe</td><td>«.-Fe</td><td><-fe</td><td>«—Fe</td>
<td>X</td><td>X</td><td></td><td>X</td><td>X</td><td>X</td><td></td><td>X</td><td></td><td>X</td>
<td>CM</td><td>CM</td><td></td><td>CM</td><td>CM</td><td>CM</td><td>Ch</td><td>CM</td><td>CM</td><td>CM</td>
<td>fe</td><td>fe</td><td></td><td>fe</td><td>fe</td><td>fe</td><td>fe</td><td>fe</td><td>fe</td><td>fe</td>
<td>T></td><td>Ό</td><td>O</td><td>Ό</td><td>• ϋ</td><td>Ό</td><td>tf</td><td>ε.</td><td>Ό</td><td></td>
<td>Fri— *</td><td>fe- *</td><td>O</td><td>Fri— *</td><td>Fri— *</td><td>fe— '</td><td>Fri— *</td><td></td><td>χ- *</td><td></td>
<td>o</td><td>o</td><td>rH</td><td>o</td><td>to</td><td>o</td><td>o</td><td>o</td><td>o</td><td>o</td>
<td>r * ·</td><td>r *</td><td></td><td>r *</td><td>LO</td><td>r-</td><td>LO</td><td> 00</td><td>LO</td><td> 00</td>
<td>fe</td><td>fe</td><td>σ></td><td> **</td><td>fe</td><td>fe</td><td>fe</td><td>fe</td><td>fe</td><td>fe</td>
<td></td><td></td><td>σ></td><td></td><td>- ^ r</td><td></td><td></td><td>vo</td><td></td><td>LO</td>
CM
I
X c
LO
CJ
Cc ti
<td>CM</td><td></td><td></td><td></td><td></td><td></td><td>C</td><td></td>
<td> 1</td><td></td><td></td><td></td><td></td><td></td><td> 0</td><td></td>
<td> 0</td><td>s</td><td></td><td></td><td></td><td></td><td></td><td> £</td>
<td><U</td><td> 1</td><td></td><td> 1</td><td> 1</td><td> 1</td><td>X</td><td> 1</td>
<td>rH</td><td></td><td></td><td></td><td></td><td></td><td>G</td><td></td>
<td>Ή</td><td></td><td></td><td></td><td></td><td></td><td> 0</td><td></td>
<td>c</td><td></td><td></td><td></td><td></td><td></td><td>r-H</td><td></td>
<td> 0</td><td></td><td></td><td></td><td></td><td></td><td>X</td><td></td>
<td>G</td><td></td><td></td><td></td><td></td><td></td><td> 0</td><td></td>
<td>C</td><td></td><td></td><td></td><td></td><td></td><td> 1</td><td></td>
<td>X</td><td></td><td></td><td></td><td></td><td></td><td>X</td><td></td>
<td></td><td></td><td></td><td></td><td>cn</td><td></td><td>X</td><td></td>
<td></td><td></td><td></td><td></td><td> 0</td><td></td><td> 0</td><td></td>
<td>co</td><td></td><td>’ŠT</td><td></td><td> 0</td><td></td><td> 0</td><td></td>
<td> 1</td><td></td><td> 1</td><td></td><td>rH</td><td></td><td>rH</td><td></td>
<td> 0</td><td></td><td> 0</td><td></td><td>•H</td><td></td><td>•H</td><td></td>
<td> 0</td><td></td><td> 0</td><td></td><td>c</td><td></td><td>c</td><td></td>
<td>r-H</td><td></td><td>i—1</td><td></td><td> 0</td><td></td><td> 0</td><td></td>
<td>•H</td><td></td><td>Ή</td><td></td><td>G</td><td></td><td>G</td><td></td>
<td>c</td><td></td><td>G</td><td></td><td>•H</td><td></td><td>•H</td><td></td>
<td> 0</td><td> 1</td><td>f3</td><td> 1</td><td>CM</td><td> 1</td><td>CM</td><td> 1</td>
<td>G Ή</td><td>Ί</td><td>G •H</td><td>Ί</td><td>0 Ή</td><td>Ί</td><td>0 •H</td><td>Ί</td>
<td>o.</td><td></td><td>CM</td><td></td><td>X</td><td></td><td>X</td><td></td>
<td> 0</td><td></td><td>O</td><td></td><td>o</td><td></td><td>o</td><td></td>
<td>G</td><td></td><td>G</td><td></td><td>G</td><td></td><td>G</td><td></td>
<td>Ό</td><td></td><td>Ό</td><td></td><td> •3</td><td></td><td>Ό</td><td></td>
<td>•rH X</td><td></td><td>•H X</td><td></td><td>Ή X</td><td></td><td>•«H X</td><td></td>
<td>0 G</td><td></td><td>(3 G</td><td></td><td>0 G</td><td></td><td>0 G</td><td></td>
<td>X</td><td></td><td>X</td><td></td><td>X</td><td></td><td>X</td><td></td>
<td> 0</td><td></td><td> 0</td><td></td><td> 0</td><td></td><td> 0</td><td></td>
<td>X</td><td></td><td>X</td><td></td><td>X</td><td></td><td>X</td><td></td>
<td></td><td> 0</td><td></td><td> 0</td><td></td><td> 0</td><td></td><td> 0</td>
<td></td><td> 0</td><td></td><td> 0</td><td></td><td> 0</td><td></td><td> 0</td>
<td> 0</td><td><-H</td><td> 0</td><td>r-H</td><td> 0</td><td>rH</td><td> 0</td><td>rH</td>
<td> 0</td><td>-H</td><td> 03</td><td>•H</td><td>Π3</td><td>Ή</td><td><ū</td><td>•rH</td>
<td>i-H</td><td>CM</td><td>rH</td><td>CM</td><td>r-H</td><td>CM</td><td>rH</td><td>CM</td>
<td>•rH</td><td>O</td><td>•H</td><td>O</td><td>H</td><td>O</td><td>•rH</td><td>O</td>
<td>X</td><td>G</td><td>X</td><td>G</td><td>X</td><td>G</td><td>X</td><td>G</td>
<td> 0</td><td>CM</td><td> 0</td><td>CM</td><td> 0</td><td>CM</td><td> 0</td><td>CM</td>
<td>rH</td><td>CM</td><td>m</td><td>sr</td><td>X</td><td>LO</td><td>Γ</td><td> 00</td>
<td>O</td><td>O</td><td>o</td><td>o</td><td>o</td><td>o</td><td>o</td><td>o</td>
<td>LO</td><td>LO</td><td>X</td><td>LO</td><td>X</td><td>X</td><td>X</td><td>X</td>
U o
-P
G >1
G
O •3 •H
Ή
N •H
MH oi
<td>ττ</td><td colspan="3">Lf)</td><td colspan="2">LO</td>
<td>rH</td><td></td><td>CH</td><td></td><td>O</td><td></td>
<td>rH</td><td> 00</td><td>rH</td><td>CH</td><td>rH</td><td> 00</td>
<td> 1</td><td>LO</td><td> 1</td><td>Γ-</td><td> 1</td><td> 00</td>
<td>CN</td><td> 1</td><td>n</td><td> 1</td><td></td><td> 1</td>
<td>rH</td><td>r-</td><td>CH</td><td>O</td><td>o</td><td>Lf)</td>
<td>rH</td><td>LO</td><td>rH</td><td>r-~</td><td>rH</td><td> 00</td>
I 31
O rH r- «-
<td colspan="2">LO</td><td colspan="5">P p</td>
<td>K</td><td></td><td></td><td>(M</td><td></td><td></td><td></td>
<td></td><td></td><td></td><td>rH</td><td></td><td></td><td></td>
<td>K</td><td></td><td></td><td></td><td></td><td></td><td></td>
<td>rH</td><td></td><td></td><td>kO</td><td></td><td></td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td></td>
<td>ε</td><td></td><td></td><td></td><td></td><td></td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td></td>
<td>o</td><td></td><td></td><td>E</td><td>E</td><td></td><td></td>
<td>m</td><td></td><td></td><td>CH</td><td>CO</td><td></td><td></td>
<td>K</td><td></td><td></td><td>K</td><td>K</td><td></td><td></td>
<td>kO</td><td></td><td></td><td>P</td><td>ε.</td><td></td><td></td>
<td> |</td><td></td><td></td><td>'—r</td><td></td><td></td><td></td>
<td>o</td><td></td><td></td><td>Γ-</td><td>o</td><td></td><td></td>
<td>rH</td><td></td><td></td><td>ΙΟ</td><td>CH</td><td></td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td></td>
<td>kO</td><td></td><td></td><td></td><td>r-</td><td></td><td></td>
<td></td><td></td><td></td><td></td><td>X.</td><td></td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td></td>
<td>E</td><td>E</td><td></td><td>E</td><td>E</td><td></td><td></td>
<td>CH</td><td>LO</td><td></td><td>CH</td><td>rH</td><td></td><td></td>
<td></td><td>«k</td><td></td><td></td><td>K</td><td>lf)</td><td></td>
<td>p</td><td>ε</td><td></td><td>e</td><td>P</td><td>CO</td><td></td>
<td></td><td></td><td>o</td><td></td><td> —</td><td>rH</td><td>lf)</td>
<td>Lf)</td><td>o</td><td>σι</td><td>o</td><td>CO</td><td> 1</td><td>σ</td>
<td>LO</td><td>CH</td><td> 1</td><td>σ</td><td>LO</td><td> 00</td><td> 1</td>
<td></td><td></td><td>r-</td><td></td><td></td><td>CN</td><td>CH</td>
<td></td><td>r-J</td><td>CD</td><td>n</td><td>LO</td><td>rH</td><td>σ</td>
<td>CH 1</td><td> 1</td><td> 1</td><td>CH 1</td><td> 1</td><td> 1</td><td> 1</td><td>co 1</td>
<td>G</td><td>Ί</td><td>Ί</td><td>G</td><td>Ί</td><td>Ί</td><td>Ί</td><td>G</td>
<td>G</td><td></td><td></td><td>G</td><td></td><td></td><td></td><td>G</td>
<td>i—1</td><td></td><td></td><td>rH</td><td></td><td></td><td></td><td>rH</td>
<td>-G</td><td></td><td></td><td>-G</td><td></td><td></td><td></td><td>-G</td>
<td>G</td><td></td><td></td><td>G</td><td></td><td></td><td></td><td>G</td>
<td>Φ</td><td></td><td></td><td>Φ</td><td></td><td></td><td></td><td>Φ</td>
<td>•H</td><td></td><td></td><td>-G</td><td></td><td></td><td></td><td>-G</td>
<td>P</td><td></td><td></td><td>P</td><td></td><td></td><td></td><td>P</td>
G >1
G
Ή
G ar
P
G •φ rH
d) P c Φ l—I
Lf) rG (4 m
i
G
<td colspan="2">co 1</td><td> 1</td><td> 1</td><td>G rH</td>
<td>G</td><td></td><td>G</td><td>G</td><td>•G</td>
<td>G</td><td></td><td>G</td><td>G</td><td>c</td>
<td>rH</td><td></td><td> 1—1</td><td> '—1</td><td>G</td>
<td>•G</td><td></td><td>•G</td><td>G</td><td>G</td>
<td>G</td><td></td><td>C</td><td>C</td><td>•G</td>
<td>G</td><td> 1</td><td>G</td><td>G</td><td>et</td>
<td>G</td><td></td><td>G</td><td>G</td><td> 0</td>
<td>•G</td><td>Ί</td><td>-G</td><td>•G</td><td>Ή</td>
<td>Ct</td><td></td><td>ft</td><td>et</td><td>P</td>
<td> 0</td><td></td><td> 0</td><td> 0</td><td> 0</td>
<td>G</td><td></td><td>G</td><td>G</td><td>G</td>
<td>P</td><td></td><td>P</td><td>P</td><td>P</td>
<td>•G</td><td></td><td>Ή</td><td>•G</td><td>•H</td>
<td>Jį</td><td></td><td>E</td><td>E</td><td>E</td>
<td> <3</td><td></td><td>G</td><td>G</td><td> 73</td>
<td>G</td><td></td><td>G</td><td>G</td><td>G</td>
<td>P</td><td></td><td>P</td><td>P</td><td>P</td>
<td>Φ</td><td></td><td>Φ</td><td>Φ</td><td>Φ</td>
<td>P</td><td></td><td>P</td><td>P</td><td>P</td>
<td>G</td><td colspan="2">C0</td><td>’S*</td>
<td>G</td><td> 1</td><td></td><td> 1</td>
<td>i—1</td><td>G</td><td></td><td>G</td>
<td>-G</td><td>G</td><td></td><td>G</td>
<td>C</td><td>i—1</td><td></td><td>i—1</td>
<td>Φ</td><td>•G</td><td></td><td>•G</td>
<td> 4-4</td><td>C</td><td></td><td>C</td>
<td> >—1</td><td>G</td><td> 1</td><td>G</td>
<td>•G</td><td>G</td><td></td><td>G</td>
<td>P</td><td>-G</td><td>Ί</td><td>-G</td>
<td></td><td>et</td><td></td><td>et</td>
<td>ε</td><td>o</td><td></td><td>o</td>
<td>•G</td><td>G</td><td></td><td>G</td>
<td>G</td><td>P</td><td></td><td>P</td>
<td>P t</td><td>•rH</td><td></td><td>•rH</td>
<td>1 LO</td><td></td><td></td><td></td>
<td></td><td>G</td><td></td><td>G</td>
<td></td><td>P</td><td></td><td>P</td>
<td></td><td>Φ</td><td></td><td>Φ</td>
<td>CN</td><td>P</td><td></td><td>P</td>
<td></td><td>G</td><td></td><td>G</td><td></td><td>G</td><td></td><td></td><td>G</td><td></td><td>G</td>
<td></td><td>G</td><td></td><td>G</td><td></td><td>G</td><td></td><td></td><td>G</td><td></td><td>G</td>
<td>G</td><td></td><td>G</td><td>rH</td><td>G</td><td>r—1</td><td>G</td><td>G</td><td>r—I</td><td>G</td><td>rH</td>
<td> 03</td><td>•H</td><td>oj</td><td>•H</td><td> 03</td><td>•rH</td><td> 03</td><td> (0</td><td>•H</td><td> 03</td><td>•r|</td>
<td>rH</td><td> 0.</td><td>rH</td><td>et</td><td>rH</td><td>et</td><td>rH</td><td>rH</td><td>et</td><td>rH</td><td>et</td>
<td></td><td>o</td><td>•H</td><td>σ</td><td>•H</td><td>o</td><td>•H</td><td>•H</td><td> 0</td><td>•H</td><td> 0</td>
<td>P</td><td>G</td><td>P</td><td>G</td><td>P</td><td>G</td><td>P</td><td>P</td><td>G</td><td>P</td><td>G</td>
<td>Φ</td><td>α</td><td>Φ</td><td>et</td><td>Φ</td><td>et</td><td>Φ</td><td>Φ</td><td>et</td><td>Φ</td><td>et</td>
<td>σ</td><td>O</td><td>rH</td><td>CH</td><td>co</td><td></td><td>lf)</td><td>LO</td><td>r-</td><td> 00</td><td>σ</td>
<td>o</td><td>r—1</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td>
<td>lf)</td><td>lf)</td><td>lf)</td><td>lf)</td><td>m</td><td>m</td><td>Lf)</td><td>Lf)</td><td>lf)</td><td>LO</td><td>lf,</td>
5.20 etilas tetrahidrotiopiranilas-3 - 79-81
T3 >1 —I
Ό £
tn
C o
% •rd tO •rd c
Ή λ:
•1-1
N
C\J
<td colspan="2"> 35</td>
<td>r-d</td><td></td>
<td>K</td><td>X</td>
<td>CO</td><td>i—d</td>
<td></td><td>·»—r</td>
<td>LO</td><td>LO</td>
<td>O</td><td>O</td>
<td>K</td><td>K</td>
<td>r-</td><td>Γ</td>
(0
K) cn <6 m
o σ
co
35
<td></td><td colspan="2">o 1~H</td><td>LO O</td><td>CN r-H</td><td colspan="3">-d</td><td colspan="2">*r (N</td><td colspan="2"></td><td>00 ’T</td>
<td>σ></td><td>T—t</td><td>T~d</td><td>rH</td><td>t—l</td><td></td><td>o</td><td>'—r</td><td>rH</td><td>o</td><td>•LT</td><td></td><td>i—d</td>
<td>co</td><td></td><td> 1</td><td> 1</td><td> 1</td><td>r-</td><td> 00</td><td>o</td><td> 1</td><td>σ</td><td>r-</td><td>o</td><td> 1</td>
<td> 1</td><td> 1</td><td> 00</td><td>’T</td><td>r-H</td><td> 1</td><td> 1</td><td></td><td>CM</td><td> 1</td><td> 1</td><td>r-</td><td>kO</td>
<td>co</td><td>o</td><td>o</td><td>o</td><td>r-H</td><td>LT)</td><td> 00</td><td></td><td>CM</td><td>co</td><td>CM</td><td></td><td>’T</td>
<td> 00</td><td>r~</td><td>rH</td><td>rH</td><td>rH</td><td>r-</td><td></td><td>kO</td><td>rH</td><td>co</td><td>Γ'</td><td>kO</td><td>r-Ί</td>
CM
I cn (0
C
Φ •rd
4-1 rH •rd
4->
CM
I cn (0 i—I H C Φ •H 4-1
CM
I tn (0 c
Φ •rd
4-1 £
O μ
n
I n
i tn tO i-1
H
τ) •rd •rd cn >1
C
Ή tn
Φ·
4-1 tn
Φ <-M
Φ
4->
C
Φ
<td>LO</td><td></td><td></td><td></td><td></td><td>LD</td><td>•5J·</td><td></td><td></td><td></td><td></td><td></td><td>CL</td>
<td></td><td></td><td></td><td></td><td>Cn</td><td>Cn</td><td></td><td></td><td></td><td></td><td>cn</td><td></td><td></td>
<td></td><td></td><td></td><td></td><td>cn</td><td>cn</td><td></td><td></td><td></td><td></td><td>cn</td><td></td><td></td>
<td>O</td><td></td><td></td><td></td><td>Φ</td><td> <0</td><td>O</td><td></td><td>’T</td><td></td><td> (0</td><td></td><td></td>
<td> 1</td><td></td><td> 1</td><td></td><td><-H</td><td></td><td> 1</td><td></td><td> 1</td><td></td><td>i-H</td><td></td><td></td>
<td>tn</td><td></td><td>tn</td><td></td><td>•rd</td><td>•rd</td><td>cn</td><td></td><td>cn</td><td></td><td>•rd</td><td></td><td></td>
<td> <0</td><td></td><td> <0</td><td></td><td>c</td><td>C5</td><td> (0</td><td></td><td>to</td><td></td><td>C</td><td></td><td></td>
<td>r-H</td><td></td><td>r-d</td><td></td><td> <0</td><td>Φ</td><td>r-H</td><td></td><td>»-H</td><td></td><td>to</td><td></td><td></td>
<td>•rd</td><td></td><td>•rd</td><td></td><td>μ</td><td>μ</td><td>•rd</td><td></td><td>•rd</td><td></td><td>μ</td><td></td><td></td>
<td>C</td><td></td><td>r*</td><td></td><td>H</td><td>-H</td><td> <—*</td><td></td><td>L-r</td><td></td><td>Ή</td><td></td><td></td>
<td>d</td><td> 1</td><td> 13</td><td></td><td>a</td><td>a</td><td> 10</td><td> 1</td><td> (0</td><td> 1</td><td>CL</td><td> 1</td><td> 1</td>
<td>μ</td><td> -</td><td>μ</td><td> -</td><td> 0</td><td>o</td><td>μ</td><td> -</td><td>μ</td><td>w</td><td>O</td><td> •</td><td></td>
<td>•rd</td><td> 1</td><td> rd</td><td> 1</td><td> rd</td><td>Ή</td><td>•rd</td><td> 1</td><td>-rd</td><td></td><td>•H</td><td> 1</td><td> 1</td>
<td>Cl,</td><td></td><td>cl</td><td></td><td> 4-1</td><td>-U</td><td>CL</td><td></td><td>CL</td><td></td><td> 4-></td><td></td><td></td>
<td> 0</td><td></td><td> 0</td><td></td><td> 0</td><td> 0</td><td> 0</td><td></td><td> 0</td><td></td><td> 0</td><td></td><td></td>
<td>μ</td><td></td><td>jh</td><td></td><td>μ</td><td>μ</td><td>μ</td><td></td><td>μ</td><td></td><td>μ</td><td></td><td></td>
<td>Ό</td><td></td><td>Ti</td><td></td><td>T!</td><td>T!</td><td>Ti</td><td></td><td>Ti</td><td></td><td>Ti</td><td></td><td></td>
<td>•H</td><td></td><td>•rd</td><td></td><td>Ή</td><td>Ή</td><td>•rd</td><td></td><td>•rd</td><td></td><td>•rd</td><td></td><td></td>
<td>X</td><td></td><td>X</td><td></td><td>X</td><td> £5</td><td> £5</td><td></td><td> £5</td><td></td><td> £5</td><td></td><td></td>
<td> <0</td><td></td><td>rd</td><td></td><td> <0</td><td> <0</td><td>tO</td><td></td><td> (0</td><td></td><td>tO</td><td></td><td></td>
<td>μ</td><td></td><td>μ</td><td></td><td>μ</td><td>μ</td><td>μ</td><td></td><td>μ</td><td></td><td>μ</td><td></td><td></td>
<td> 4-1</td><td></td><td>4J</td><td></td><td> 4-1</td><td> 4-1</td><td> 4-1</td><td></td><td> 4-1</td><td></td><td> 4-1</td><td></td><td></td>
<td>φ</td><td></td><td>φ</td><td></td><td>Φ</td><td>Φ</td><td>Φ</td><td></td><td>φ</td><td></td><td>Φ</td><td></td><td></td>
<td> 4-)</td><td></td><td> 4-1</td><td></td><td> 4-1</td><td> 4-1</td><td> 4-1</td><td></td><td>X</td><td></td><td> £1</td><td></td><td></td>
<td></td><td>cn</td><td></td><td>cn</td><td></td><td>cn</td><td></td><td>cn</td><td></td><td>w</td><td></td><td>cn</td><td></td>
<td></td><td> (0</td><td></td><td> (0</td><td></td><td> (0</td><td></td><td> (0</td><td></td><td> (0</td><td></td><td> (0</td><td></td>
<td>cn</td><td>r-H</td><td>tn</td><td>r-H</td><td>cn</td><td>r-H</td><td>cn</td><td>rH</td><td>tn</td><td>r-H</td><td>tn</td><td>t—1</td><td>cn</td>
<td>Φ</td><td>•rd</td><td>tO</td><td>•rd</td><td> (0</td><td>•H</td><td>to</td><td>•rd</td><td>tū</td><td>•μ</td><td>tO</td><td>•rd</td><td> (0</td>
<td>r-H</td><td>X</td><td>r-H</td><td>α</td><td>r-H</td><td>CL</td><td>r-H</td><td>CL</td><td>r-H</td><td>CL</td><td>r-d</td><td>CL</td><td>r“H</td>
<td>•H</td><td>o</td><td>•rd</td><td> 0</td><td>•H</td><td>o</td><td>Ή</td><td> 0</td><td>•rd</td><td>O</td><td>•rd</td><td>O</td><td>•H</td>
<td> 4-></td><td>μ</td><td> 4-1</td><td>μ</td><td> 4-1</td><td>μ</td><td> 4-1</td><td>μ</td><td> 4-1</td><td>μ</td><td> 4-1</td><td>μ</td><td>X</td>
<td>Φ</td><td>CL</td><td>Φ</td><td>CL</td><td>Φ</td><td>CL</td><td>Φ</td><td>Ω.</td><td>Φ</td><td>CL</td><td>Φ</td><td>CL</td><td>Φ</td>
<td>CM</td><td>m</td><td>’T</td><td>LO</td><td> <0</td><td>r-</td><td> 00</td><td> <7\</td><td>O</td><td>r-H</td><td>CM</td><td>co</td><td>’T</td>
<td>CM</td><td>CM</td><td>CM</td><td>CM</td><td>CM</td><td>CM</td><td>CM</td><td>CM</td><td>cn</td><td>ΓΟ</td><td>CO</td><td>cn</td><td>cn</td>
5.35 propilas tetrahidropiranilas-3 piridilas-3 6,40(dt,lH), 7,30(7,75, 8,408,70(3m,4H)
I I
<td colspan="2"></td><td colspan="2">O M<sup>1</sup> 00</td><td colspan="2">o 00</td>
<td></td><td></td><td></td><td></td><td>ta.</td><td></td>
<td></td><td></td><td>LD</td><td></td><td>LO</td><td></td>
<td></td><td></td><td>r-</td><td></td><td>r-</td><td></td>
<td></td><td></td><td>K</td><td></td><td></td><td></td>
<td></td><td></td><td>r-</td><td></td><td>r-</td><td></td>
<td></td><td></td><td>K</td><td></td><td></td><td></td>
<td></td><td></td><td>o</td><td></td><td>o</td><td></td>
<td></td><td></td><td>co</td><td></td><td>ΓΌ</td><td></td>
<td></td><td></td><td>ta.</td><td></td><td>ta.</td><td></td>
<td></td><td></td><td>r*·</td><td></td><td>r-</td><td></td>
<td></td><td></td><td>ta.</td><td></td><td></td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td>
<td></td><td></td><td>X</td><td></td><td></td><td>E</td>
<td></td><td></td><td>r-f</td><td>sr</td><td>r-H</td><td>*r</td>
<td></td><td></td><td></td><td></td><td></td><td></td>
<td>UO</td><td></td><td> 4-></td><td>g</td><td>-P</td><td>e</td>
<td>LO</td><td></td><td>S</td><td>co</td><td>τί</td><td>m</td>
<td>r-)</td><td> 00</td><td></td><td></td><td></td><td></td>
<td> 1</td><td>r~-</td><td>O</td><td>o</td><td>o</td><td>o</td>
<td>X</td><td> 1</td><td></td><td>r-</td><td></td><td>r-</td>
<td>LD</td><td>n</td><td></td><td>k</td><td>ta.</td><td>ta.</td>
<td></td><td>r-</td><td>LO</td><td> 00</td><td>kO</td><td> 00</td>
<td></td><td></td><td>n 1</td><td></td>
<td></td><td></td><td>1 cn</td><td></td>
<td>X</td><td></td><td>(fl</td><td></td>
<td> 1</td><td></td><td>i—t</td><td></td>
<td>n</td><td></td><td>•G</td><td></td>
<td> (0</td><td></td><td>G</td><td></td>
<td>r-”t</td><td></td><td> 3</td><td></td>
<td>Ή</td><td></td><td>G</td><td></td>
<td>C</td><td></td><td>-G</td><td></td>
<td> <3</td><td> 1</td><td>a</td><td> 1</td>
<td>M •H</td><td> =</td><td>o •G</td><td>Ί</td>
<td>a</td><td></td><td>X</td><td></td>
<td>o G</td><td></td><td>o G</td><td></td>
<td>X Ή</td><td></td><td>X -G</td><td></td>
•H -H
G G
<td>X</td><td>X</td>
<td>cu</td><td>(U</td>
<td>X</td><td>X</td>
<td></td><td>cn</td><td></td><td>cn</td>
<td></td><td>(fl</td><td></td><td>(C</td>
<td>cn</td><td>X</td><td> «</td><td>t—1</td>
<td>(fl</td><td>•G</td><td>fŪ</td><td>•G</td>
<td> '—1</td><td>a</td><td>•H</td><td>a</td>
<td>G</td><td>o</td><td>•H</td><td> 0</td>
<td>X</td><td>G</td><td>X</td><td>G</td>
<td>cu</td><td>a</td><td>(U</td><td>a</td>
<td>LD</td><td></td><td> 00</td><td>cn</td>
<td>co</td><td>co</td><td>co</td><td>co</td>
<td> •</td><td> •</td><td> •</td><td> •</td>
<td>m</td><td>m</td><td>m</td><td>uo</td>
(M
I «
(0 σι l
Γ σ
<td> 35</td><td></td><td>K</td><td></td><td></td>
<td>n</td><td></td><td>co</td><td> 35</td><td> 35</td>
<td></td><td></td><td></td><td>cn</td><td>n</td>
<td>ε</td><td></td><td>ε</td><td>a</td><td> *.</td>
<td>CM</td><td></td><td>CM</td><td>ε</td><td>ε</td>
<td> ’*—*·</td><td></td><td> *>—*</td><td> *—*</td><td></td>
<td>o</td><td></td><td>o</td><td>o</td><td>o</td>
<td>m</td><td></td><td> 00</td><td>*T</td><td></td>
<td>K</td><td></td><td></td><td></td><td>K</td>
<td>r- i</td><td></td><td>r- I</td><td>r- I</td><td>r- |</td>
<td>1 o</td><td></td><td>1 O</td><td>1 O</td><td>1 O</td>
<td>σ></td><td></td><td>σ></td><td>O</td><td>o</td>
<td></td><td></td><td></td><td>*a</td><td> <</td>
<td>kO</td><td></td><td>kO</td><td>r-</td><td>r-</td>
<td> *»</td><td></td><td></td><td> *»</td><td></td>
<td></td><td></td><td>^—a.</td><td></td><td>a»</td>
<td>K</td><td></td><td> 35</td><td> 35</td><td></td>
<td>t-4</td><td></td><td>tH</td><td>r”4</td><td>r~1</td>
<td>•a</td><td></td><td>K</td><td></td><td>K</td>
<td></td><td></td><td>n</td><td>m</td><td>w</td>
<td> *»->*</td><td>o</td><td></td><td> '·*’</td><td>'a-’</td>
<td>LO</td><td>σ</td><td>tn</td><td>o</td><td>o</td>
<td>kO</td><td> 1</td><td>co</td><td>cn</td><td>LO</td>
<td>K</td><td> 00</td><td>K</td><td>K</td><td> *»</td>
<td>kO</td><td> 00</td><td>co</td><td>co</td><td>kO</td>
o σ
ι oo oo
Φ
P
C
Φ
NO-CH^C =CH-W et cn (0 —4 •r4
C (0 p
<img file="LT3295B_D0017.tif" />
I <M x
I tS3
II s
o •c4
r.
to
M
P
Φ
P m
<ΰ
<td>1 1 Ί Ί</td><td>i 1 Ί Ί</td><td>co <sup>1</sup>J) <sup>s</sup>> (0 t—1 •P c Φ -P P</td><td>co 1 m <ΰ 1—1 P d Φ •P P</td>
<td></td><td>CO</td><td></td><td></td>
<td></td><td>1 tn</td><td></td><td></td>
<td><r</td><td>fŪ</td><td>co</td><td>'T</td>
<td> 1</td><td>t—4</td><td> 1</td><td> 1</td>
<td>cn</td><td>•r4</td><td> 9)</td><td> «</td>
<td> (0</td><td>G</td><td> (0</td><td> (0</td>
<td>Ip</td><td> 3</td><td> 1—1</td><td>i—1</td>
<td>•H</td><td>M</td><td>-P</td><td>P</td>
<td>C</td><td>•r4</td><td> £5</td><td>d</td>
<td>S i</td><td>Ch 1</td><td>f3 1</td><td>ϊ3</td>
<td>K = •P 1</td><td>0 - •H |</td><td>p s •P 1</td><td>P •P</td>
<td>a</td><td>4J</td><td>sx</td><td></td>
<td> 0</td><td> 0</td><td>o</td><td> 0</td>
<td>P</td><td>M</td><td>P</td><td>P</td>
<td> 73</td><td>Ό</td><td>Ό</td><td>U</td>
<td>Ή</td><td>Ή</td><td>•r4</td><td>•P</td>
<td> 35</td><td>Jį</td><td> 35</td><td> 35</td>
<td> (0</td><td> (0</td><td> (3</td><td> (3</td>
<td>M</td><td>P</td><td>P</td><td>P</td>
<td>P</td><td>P</td><td>P</td><td>P</td>
<td>Φ</td><td>Φ</td><td>φ</td><td>Φ</td>
<td>P</td><td>P</td><td>P</td><td>P</td>
<td colspan="2">cn</td><td colspan="2">cn</td><td>cn</td><td colspan="3">cn</td>
<td> <0</td><td></td><td>Φ</td><td></td><td>Φ</td><td></td><td> <0</td><td></td>
<td></td><td>cn</td><td>f-d</td><td>cn</td><td>—i</td><td>cn</td><td>i—1</td><td>w</td>
<td>•r4</td><td>Φ</td><td> •<4</td><td>Φ</td><td>H</td><td>Φ</td><td>•P</td><td>d</td>
<td>a</td><td>i—1</td><td> 0.</td><td> *—1</td><td>ft</td><td> »—1</td><td>(X</td><td>r-4</td>
<td> 0</td><td>-P</td><td> 0</td><td>•P</td><td>o</td><td>P</td><td>o</td><td>•r4</td>
<td>P</td><td>P</td><td>P</td><td>P</td><td>P</td><td>P</td><td>P</td><td>-P</td>
<td>a</td><td>Φ</td><td>d</td><td>Φ</td><td>cx</td><td>Φ</td><td>£X</td><td><D</td>
o
<td>CM</td><td>co</td><td></td><td>LO</td><td>kO</td><td>r-</td><td> 00</td><td><Ti</td>
<td>O</td><td>O</td><td>o</td><td>O</td><td>o</td><td>o</td><td>o</td><td>o</td>
H cP
J
<td> 2</td><td> 2</td><td> 2</td><td></td><td> 2</td><td></td><td> 2</td><td></td><td> 2</td><td></td><td></td><td></td><td></td><td></td>
<td>co</td><td>co</td><td>co</td><td></td><td>CM</td><td></td><td>CM</td><td></td><td>CM</td><td></td><td></td><td></td><td></td><td></td>
<td>fe</td><td>fe</td><td>fe</td><td></td><td>fe</td><td></td><td>fe</td><td></td><td>fe.</td><td></td><td></td><td></td><td></td><td></td>
<td>E:</td><td>Eį</td><td> £;</td><td></td><td>ε</td><td></td><td>ε</td><td></td><td>ε</td><td></td><td></td><td></td><td></td><td></td>
<td></td><td></td><td></td><td></td><td>M·»»</td><td></td><td> ***·</td><td></td><td> *—*</td><td></td><td>>*fe.</td><td></td><td></td><td></td>
<td>o</td><td>o</td><td>o</td><td></td><td>O</td><td></td><td>o</td><td></td><td>o</td><td></td><td>K</td><td></td><td></td><td></td>
<td> *3*</td><td>M*</td><td>Ν’</td><td></td><td>o</td><td></td><td>o</td><td></td><td>o</td><td></td><td>CM</td><td></td><td></td><td></td>
<td>fe.</td><td>fe.</td><td></td><td></td><td>fe</td><td></td><td>fe</td><td></td><td>s</td><td></td><td>fe</td><td></td><td></td><td></td>
<td>r-</td><td>Γ-</td><td></td><td></td><td>r*</td><td></td><td>r*</td><td></td><td>r-</td><td></td><td>ε</td><td></td><td></td><td></td>
<td> |</td><td>l</td><td>i</td><td></td><td> 1</td><td></td><td>I</td><td></td><td> 1</td><td></td><td> *—*</td><td></td><td></td><td></td>
<td>O</td><td>o</td><td>o</td><td></td><td>m</td><td></td><td>tn</td><td></td><td>o</td><td></td><td>o</td><td></td><td></td><td></td>
<td>o</td><td>o</td><td>o</td><td></td><td>kO</td><td></td><td>kO</td><td></td><td>kO</td><td></td><td>cr></td><td></td><td></td><td></td>
<td> •</td><td>fe</td><td></td><td></td><td> *.</td><td></td><td>fe.</td><td></td><td>fe</td><td></td><td>fe</td><td></td><td></td><td></td>
<td>r-</td><td>r*</td><td>r-</td><td></td><td>LO</td><td></td><td>LO</td><td></td><td>kO</td><td></td><td>kO</td><td></td><td></td><td></td>
<td></td><td> ·»</td><td>fe</td><td></td><td>fe</td><td></td><td>fe</td><td></td><td>fe</td><td></td><td>fe</td><td></td><td></td><td></td>
<td></td><td> ,»—»«»</td><td></td><td></td><td>,^-fe</td><td></td><td>^-•fe</td><td></td><td>>—fe</td><td></td><td></td><td></td><td></td><td></td>
<td>te</td><td>K</td><td>te</td><td></td><td>ac</td><td></td><td>K</td><td></td><td>X</td><td></td><td>K</td><td></td><td></td><td></td>
<td>r-H</td><td>rH</td><td>rH</td><td></td><td>rH</td><td></td><td>rH</td><td></td><td>rH</td><td></td><td>rH</td><td></td><td></td><td></td>
<td>fe</td><td>fe</td><td>fe</td><td>o</td><td></td><td>CM</td><td>fe</td><td>o</td><td>fe</td><td></td><td>fe.</td><td>LO</td><td></td><td>LD</td>
<td>cn</td><td>cn</td><td>cn</td><td>rH</td><td>cn</td><td>t-H</td><td>cn</td><td><N</td><td>cn</td><td></td><td>cn</td><td>CM</td><td></td><td>O</td>
<td></td><td> *—·</td><td> *—*</td><td>rH</td><td>'-r'</td><td>rH</td><td> ·*-*·</td><td>«—H</td><td>fe—X</td><td>LD</td><td></td><td>r—l</td><td> 00</td><td>rH</td>
<td>tn</td><td>m</td><td>o</td><td>i</td><td>o</td><td> 1</td><td>o</td><td> 1</td><td>tn</td><td> 00</td><td>o</td><td> 1</td><td>cn</td><td> 1</td>
<td>tn</td><td>tn</td><td>tn</td><td> 00</td><td>kO</td><td>rH</td><td>kO</td><td><n</td><td>tn</td><td> 1</td><td>r·</td><td>T</td><td>l</td><td>cn</td>
<td></td><td></td><td></td><td>o</td><td>fe</td><td>rH</td><td>fe</td><td>t-H</td><td></td><td>CM</td><td> ·.</td><td>CM</td><td>r-</td><td>o</td>
<td>kO</td><td> <0</td><td>kO</td><td>rH</td><td>kO</td><td>rH</td><td>kO</td><td>rH</td><td>kO</td><td> 00</td><td>kO</td><td>rH</td><td>cn</td><td>rH</td>
CM
I co
CCJ c
d) •H
4-)
I
LT)
Oi co >1
C
-rd (0 <V
4-1
CO •d) r—I
d) +J
C <v oi
LO
Fl
Z
<td>co</td><td></td><td></td><td>CO 1</td><td></td><td></td><td></td><td>CO i</td>
<td>1 co</td><td></td><td></td><td>I co</td><td></td><td></td><td></td><td>co</td>
<td>et!</td><td>CO</td><td>’T</td><td> «3</td><td></td><td></td><td>«r</td><td> 0</td>
<td>r-l</td><td> 1</td><td> 1</td><td>rH</td><td></td><td></td><td> 1</td><td>i—1</td>
<td>r-l</td><td>CO</td><td>CO</td><td>•rH</td><td></td><td></td><td>co</td><td>-r-l</td>
<td>C</td><td><a</td><td> (0</td><td>C</td><td></td><td></td><td> (0</td><td>G</td>
<td> <3</td><td>r—1</td><td> »—1</td><td>čo</td><td></td><td></td><td>i—1</td><td> <3</td>
<td>Fl</td><td>-r-l</td><td>-r-l</td><td>Fl</td><td></td><td></td><td>•H</td><td>P</td>
<td>Ή</td><td>C</td><td>c</td><td>Ή</td><td></td><td></td><td>C</td><td>•rd</td>
<td>CU 1</td><td>!3 i</td><td>et 1</td><td>P. 1</td><td> 1</td><td> 1</td><td> (0 1</td><td>P.</td>
<td>o s •P 1</td><td>F< e H |</td><td>Fi s H |</td><td>o s Ή 1</td><td>Ί</td><td>z</td><td>Fl e •Η 1</td><td>o •rH</td>
<td>4J</td><td>a</td><td>CU</td><td> 4-1</td><td></td><td></td><td>S*</td><td> 4-1</td>
<td>O</td><td> 0</td><td> 0</td><td> 0</td><td></td><td></td><td> 0</td><td> 0</td>
<td>H</td><td>Fj</td><td>Fl</td><td>Fj</td><td></td><td></td><td>P</td><td>P</td>
<td>S</td><td>H</td><td>Ό</td><td> 3</td><td></td><td></td><td>’O</td><td>Ό</td>
<td>•r-l</td><td>-H</td><td>H</td><td>r-l</td><td></td><td></td><td>•rd</td><td>•H</td>
<td></td><td></td><td>Λ ITJ</td><td></td><td></td><td></td><td></td><td></td>
<td>M</td><td>P</td><td>M</td><td>p</td><td></td><td></td><td>P</td><td>P</td>
<td> 4-1</td><td> 4-1</td><td> 4-1</td><td>4J</td><td></td><td></td><td>4J</td><td>4J</td>
<td>(U</td><td><U</td><td>(U</td><td>CU</td><td></td><td></td><td>d></td><td>d)</td>
<td>d-></td><td>-U</td><td>4J</td><td> 4-1</td><td></td><td></td><td>-P</td><td>d-></td>
<td>to</td><td></td><td>co</td><td></td><td>co</td><td></td><td>co</td><td></td><td>cn</td><td></td><td>to</td><td></td><td>CO</td><td></td>
<td>«j</td><td></td><td>ca</td><td></td><td><a</td><td></td><td><ū</td><td></td><td>ca</td><td></td><td>ca</td><td></td><td>Cū</td><td></td>
<td></td><td>cn</td><td></td><td>to</td><td>rH</td><td>CO</td><td>rH</td><td>co</td><td>r-H</td><td>co</td><td>rH</td><td>co</td><td>rH</td><td>CO</td>
<td>•H</td><td>ca</td><td>•rH</td><td>ca</td><td>•H</td><td>ca</td><td>•rH</td><td>ca</td><td>•rH</td><td>c8</td><td>•rH</td><td>ca</td><td>•rH</td><td>ca</td>
<td>P.</td><td>r-H</td><td>CU</td><td>r-l</td><td>P.</td><td>rH</td><td>CU</td><td>rH</td><td>P<</td><td>r-H</td><td>p.</td><td>r-H</td><td>P.</td><td>r-H</td>
<td>o</td><td></td><td>o</td><td>•H</td><td> 0</td><td>•ri</td><td>o</td><td>•rH</td><td>o</td><td>Ή</td><td>o</td><td>•rH</td><td> 0</td><td>•rH</td>
<td>P</td><td>-P</td><td>P</td><td>4J</td><td>P</td><td> 4-1</td><td>P</td><td> 4-1</td><td>P</td><td>-P</td><td>P</td><td>-P</td><td>P</td><td>d-></td>
<td>P.</td><td>d)</td><td>P.</td><td>Φ</td><td>P.</td><td>d)</td><td>P.</td><td>d)</td><td>cu</td><td>d)</td><td>cu</td><td><u</td><td>CU</td><td>cu</td>
<td>o</td><td>rH</td><td>CM</td><td>CO</td><td>Ν’</td><td>uo</td><td>LO</td><td>I—</td><td> 00</td><td>cn</td><td>o</td><td>rH</td><td>CM</td><td>m</td>
<td>rH</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td><td>r-H</td><td>rH</td><td>CM</td><td>CM</td><td>CM</td><td>CM</td>
LO
LO
LO
LO
LO
LO
LO
LO LO
LO
M’
CM propilas - 6,65(s,lH), 6,90(m, 2H)
LO lentelė
E r-I k
o o
k.
LO
E
CM
E rH k
ε
E rH k
o o
LO
E
CM
E rH k
ε
E rH o
o
LO
E rH k
ε
E i<sup>-</sup>1 £
O o
ki
LO
E rH
k.
ε
<td>r*</td><td>O</td><td>r-</td><td>O</td><td>k</td><td>o</td><td>k</td><td>o</td>
<td>o</td><td>CO</td><td>o</td><td>co</td><td>^-χ</td><td>co</td><td></td><td>co</td>
<td>k</td><td>kl</td><td>k</td><td>k</td><td>n:</td><td>k</td><td>X</td><td>k</td>
<td></td><td>r</td><td> <3*</td><td>r*-</td><td> <3*</td><td>r-</td><td></td><td>r*</td>
<td></td><td></td><td></td><td></td><td>X</td><td></td><td>k</td><td></td>
<td></td><td></td><td>ki</td><td>k</td><td>ε</td><td>k</td><td>ε</td><td>k</td>
<td>X</td><td>x</td><td>X</td><td>Χ—Χ,</td><td>‘k—'</td><td></td><td>k<sup>-</sup>*</td><td>X«X</td>
<td>X!</td><td>X</td><td>E</td><td></td><td>CO</td><td>E</td><td>co</td><td>E</td>
<td>CM</td><td>rH</td><td>CM</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td>
<td>k</td><td>kl</td><td>X</td><td>k</td><td>k</td><td>k</td><td>k</td><td>k</td>
<td>ε</td><td>ε</td><td>ε</td><td>ε</td><td></td><td>ε.</td><td> *3*</td><td>ε</td>
<td>k—'</td><td>k-»·</td><td>k—*</td><td>k·—·»</td><td> 1</td><td></td><td>I</td><td>k-r</td>
<td>CO</td><td>LO</td><td>co</td><td>LO</td><td>o</td><td>LO</td><td>O</td><td>LO</td>
<td>σ</td><td>CM</td><td>σ</td><td>CM</td><td>σ</td><td>CM</td><td>σ</td><td>CM</td>
<td>kl</td><td>k</td><td> •</td><td>k</td><td>k</td><td>X</td><td>X</td><td>k</td>
<td>co</td><td>LO</td><td>co</td><td>LO</td><td>co</td><td>LO</td><td>co</td><td>LO</td>
<img file="LT3295B_D0018.tif" />
.05 etilas tetrahidrotiopiranilas-3 4,06(m, 2H), 6,00(m,1H), 6,26(m,1H)
7,30(m, 1H)
τ) ė
•e •rd
Cti •H •H
N •H
<td colspan="2">k</td><td colspan="2">k</td><td colspan="8">ffi</td>
<td></td><td></td><td></td><td>^«k</td><td></td><td></td><td></td><td></td><td></td><td>rd</td><td></td><td></td>
<td>ffi</td><td></td><td></td><td>ffi</td><td></td><td></td><td></td><td></td><td></td><td>k</td><td></td><td></td>
<td>t—1</td><td></td><td></td><td>CM</td><td></td><td></td><td></td><td></td><td></td><td> 3</td><td></td><td></td>
<td>k</td><td></td><td></td><td>k</td><td></td><td></td><td></td><td></td><td></td><td>p</td><td></td><td></td>
<td>g</td><td></td><td></td><td>g</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>CO</td><td></td><td></td>
<td>uo</td><td></td><td></td><td>r*</td><td></td><td></td><td></td><td></td><td></td><td>rd</td><td>k</td><td></td>
<td>CM</td><td></td><td></td><td> 00</td><td></td><td></td><td></td><td></td><td></td><td>k</td><td>z»k</td><td></td>
<td>k</td><td></td><td></td><td>k</td><td></td><td>ffi</td><td></td><td></td><td></td><td>r-</td><td>ffi</td><td></td>
<td>uo</td><td></td><td></td><td>m</td><td></td><td>CM</td><td></td><td></td><td></td><td></td><td>rd</td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>k</td><td>k</td><td></td>
<td>k</td><td></td><td></td><td>k</td><td></td><td>g</td><td></td><td></td><td></td><td>^-k</td><td>P</td><td>ffi</td>
<td></td><td></td><td></td><td></td><td></td><td></td><td>X-k</td><td>x-k</td><td></td><td>ffi</td><td>P</td><td>rd</td>
<td>ffi</td><td></td><td></td><td>ffi</td><td></td><td>r-</td><td>ffi</td><td>ffi</td><td></td><td>rd</td><td></td><td>k</td>
<td></td><td></td><td></td><td>CM</td><td></td><td> 00</td><td>CM</td><td>CM</td><td></td><td>k</td><td>o</td><td> 3</td>
<td></td><td></td><td></td><td>k</td><td></td><td>k</td><td>k</td><td>k</td><td></td><td>P</td><td> 00</td><td>P</td>
<td>g</td><td></td><td></td><td>g</td><td></td><td>m</td><td>g</td><td>g</td><td></td><td>t)</td><td>k</td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>uo</td><td>co</td>
<td>o</td><td></td><td></td><td>r*</td><td></td><td>k</td><td>r-</td><td>r*</td><td>k</td><td>co</td><td>k</td><td>rd</td>
<td>o</td><td></td><td></td><td>o</td><td></td><td></td><td> 00</td><td> 00</td><td></td><td>σ</td><td>«^k</td><td>k</td>
<td>k</td><td></td><td></td><td>k</td><td></td><td>ffi</td><td>k</td><td>k</td><td>ffi</td><td>k</td><td>ffi</td><td>r-</td>
<td>kO</td><td></td><td></td><td>sr</td><td></td><td>sT</td><td>LO</td><td>LO</td><td>sr</td><td>kO</td><td>sr</td><td></td>
<td></td><td></td><td></td><td></td><td></td><td>k</td><td></td><td></td><td>k</td><td></td><td></td><td></td>
<td>k</td><td></td><td></td><td>k</td><td></td><td>g</td><td>k</td><td>k</td><td>g</td><td></td><td>g</td><td>^-k</td>
<td></td><td></td><td></td><td>^-k</td><td></td><td></td><td>te.</td><td>Z^-k</td><td></td><td>ffi</td><td></td><td>ffi</td>
<td>ffi</td><td>ffi</td><td></td><td>ffi</td><td></td><td>LO</td><td>ffi</td><td>ffi</td><td>lo</td><td>rd</td><td>m</td><td>rd</td>
<td>CM</td><td>1—I</td><td></td><td>CM</td><td></td><td>γ—I</td><td>CM</td><td>CM</td><td>rd</td><td>k</td><td>rd</td><td>k</td>
<td></td><td></td><td></td><td>k</td><td></td><td>k</td><td>k</td><td>k</td><td>k</td><td>P</td><td>k</td><td> 3</td>
<td>g</td><td>g</td><td></td><td>g</td><td></td><td>sr</td><td>g</td><td>g</td><td>sr</td><td>P</td><td>sr</td><td>P</td>
<td></td><td></td><td>sr</td><td></td><td> 00</td><td> |</td><td> *-*·</td><td></td><td> 1</td><td>r·</td><td> 1</td><td></td>
<td>m</td><td>o</td><td>uo</td><td>co</td><td>r-</td><td>o</td><td>r-</td><td>r-</td><td>o</td><td>o</td><td>o</td><td>co</td>
<td>o</td><td>cn</td><td>I</td><td>σ</td><td>I</td><td>σ</td><td>o</td><td>o</td><td> 00</td><td> 00</td><td> 00</td><td>σ</td>
<td>k</td><td>k</td><td>CM</td><td>k</td><td>kO</td><td>k</td><td>k</td><td>k</td><td>k</td><td>k</td><td>k</td><td>k</td>
<td>sr</td><td>r-</td><td>UO</td><td>co</td><td>r·</td><td>CO</td><td>sr</td><td>sr</td><td>co</td><td>uo</td><td>co</td><td>kO</td>
<td>CM 1</td><td>CM I</td>
<td>1 ca</td><td>ca</td>
<td>ca</td><td>fŪ</td>
<td>rd</td><td> 1—1</td>
<td>•H</td><td>•H</td>
<img file="LT3295B_D0019.tif" />
<td>G</td><td>G</td>
<td>Mm</td><td>Cffi</td>
<td>rd</td><td>rd</td>
<td>•H</td><td>•H</td>
<td>-U</td><td>ffi i</td>
<td>LO</td><td>c 1 m</td>
CM
I m
(ti rd •H
G
d) •G ffi ffi cn >1
G
-G cn ar
-g cn -d) r—t d) ffi G d) i-G ffi r-
<td></td><td colspan="8">co</td>
<td></td><td></td><td></td><td></td><td></td><td>cn</td><td></td><td></td><td></td>
<td></td><td>co</td><td>co</td><td>sr</td><td></td><td>(ū</td><td></td><td>C0</td><td></td>
<td></td><td> 1</td><td>l</td><td> 1</td><td></td><td>rd</td><td></td><td> 1</td><td></td>
<td></td><td>cn</td><td>m</td><td>cn</td><td></td><td>•rd</td><td></td><td>cn</td><td></td>
<td></td><td>d)</td><td>(ti</td><td>(d</td><td></td><td>G</td><td></td><td>fl</td><td></td>
<td></td><td>r-d</td><td>rd</td><td>rd</td><td></td><td> !3</td><td></td><td>r—1</td><td></td>
<td></td><td>rd</td><td>•rd</td><td>•rd</td><td></td><td>G</td><td></td><td>•rd</td><td></td>
<td></td><td>ς</td><td>G</td><td>G</td><td></td><td>• rd</td><td></td><td>c</td><td></td>
<td> 1</td><td>d</td><td> !3</td><td>č3</td><td> 1</td><td>A</td><td> 1</td><td> (3</td><td> 1</td>
<td></td><td>G •rd</td><td>G •rd</td><td>G •rd</td><td>Ί</td><td>O •rd</td><td>Ί</td><td>G •rd</td><td>Ί</td>
<td></td><td>(X</td><td>a</td><td>A</td><td></td><td>ffi</td><td></td><td>A</td><td></td>
<td></td><td>o</td><td>o</td><td> 0</td><td></td><td>o</td><td></td><td> 0</td><td></td>
<td></td><td>G</td><td>G</td><td>G</td><td></td><td>G</td><td></td><td>G</td><td></td>
<td></td><td>P</td><td>P</td><td>P</td><td></td><td>P</td><td></td><td>P</td><td></td>
<td></td><td>•rd ffi</td><td>•rd ffi</td><td>•rd ffi</td><td></td><td>•r| ffi</td><td></td><td>•id ffi</td><td></td>
<td></td><td><3 G</td><td>(3 G</td><td>(3 G</td><td></td><td>73 G</td><td></td><td>(3 G</td><td></td>
<td></td><td>ffi</td><td>ffi</td><td>ffi</td><td></td><td>ffi</td><td></td><td>ffi</td><td></td>
<td></td><td>d)</td><td>d)</td><td>d)</td><td></td><td>d)</td><td></td><td>d)</td><td></td>
<td></td><td>ffi</td><td>ffi</td><td>ffi</td><td></td><td>ffi</td><td></td><td>ffi</td><td></td>
<td>cn</td><td></td><td>cn</td><td></td><td>cn</td><td></td><td>cn</td><td></td><td>cn</td>
<td> (0</td><td></td><td></td><td></td><td> (0</td><td></td><td>(ū</td><td></td><td>(ti</td>
<td>rd</td><td>cn</td><td>rd</td><td>cn</td><td>rd</td><td>ca</td><td>r-d</td><td>cn</td><td>rd</td>
<td>•rl</td><td>(ti</td><td>♦rd</td><td>(C)</td><td>•rd</td><td>ai</td><td>•rd</td><td>(ti</td><td>•«d</td>
<td> &</td><td>rd</td><td>A</td><td>rd</td><td>A</td><td>rd</td><td>A</td><td>rd</td><td>A</td>
<td>o</td><td>•H</td><td>o</td><td>•rd</td><td> 0</td><td>•rd</td><td> 0</td><td>•H</td><td> 0</td>
<td>G</td><td>ffi</td><td>G</td><td>ffi</td><td>G</td><td>ffi</td><td>G</td><td>ffi</td><td>G</td>
<td>a</td><td>d)</td><td>A</td><td>d)</td><td>A</td><td>d)</td><td>A</td><td>d)</td><td>A</td>
<td>uo</td><td>Γ</td><td> 00</td><td>σ</td><td>O</td><td>rd</td><td>CM</td><td>co</td><td>*r</td>
<td>o</td><td>o</td><td>o</td><td>O</td><td>rd</td><td>rd</td><td>rd</td><td>rd</td><td>rd</td>
<td> •</td><td> •</td><td></td><td></td><td></td><td></td><td></td><td></td><td> •</td>
<td>r</td><td></td><td>r-</td><td>r~</td><td>r</td><td>Γ'</td><td></td><td>r</td><td>r</td>
. 15 etilas tetrahidropiranilas-4 tienilas-2 3,90-4,23(m, 4H), 6,80(dd,1H)
6, 93 (dd, 1H), 7,13(dd,lH) s
T)
CO σ
LO
X
S
T3 cn σ
ta
LO
<td>T)</td><td></td><td>ta</td><td></td><td>ta</td>
<td>s</td><td>K</td><td></td><td></td><td></td>
<td></td><td>r-d</td><td> 33</td><td></td><td>K</td>
<td>o</td><td>ta</td><td><-d</td><td></td><td>r—1</td>
<td> 00</td><td>Ό</td><td></td><td></td><td></td>
<td>ta</td><td>S</td><td></td><td></td><td>Ό</td>
<td>LO</td><td></td><td>ū</td><td></td><td>Ό</td>
<td></td><td>co</td><td></td><td></td><td></td>
<td>ta</td><td>r-H</td><td>o</td><td></td><td>o</td>
<td></td><td></td><td> 00</td><td></td><td> 00</td>
<td></td><td>r-</td><td>K</td><td></td><td>ta</td>
<td></td><td></td><td>kO</td><td></td><td>kO</td>
<td>ta</td><td>ta</td><td></td><td></td><td></td>
<td>M</td><td>-—s.</td><td>ta</td><td>x-ta</td><td>ta</td>
<td></td><td>K</td><td></td><td> 33</td><td>--ta.</td>
<td>m</td><td> «—1</td><td>a:</td><td>T<sup>-</sup>(</td><td>Λ</td>
<td>CM</td><td>K.</td><td>CM</td><td></td><td>CM</td>
<td></td><td>TJ</td><td>ta</td><td>Ό</td><td></td>
<td></td><td></td><td>ε.</td><td>Ό</td><td>g.</td>
<td> 1</td><td> *—>*</td><td></td><td> ·“—«*</td><td></td>
<td>o</td><td>co</td><td>LO</td><td>co</td><td>kO</td>
<td>cn</td><td>σι</td><td>O</td><td>r~4</td><td>O</td>
<td></td><td>ta</td><td>ta.</td><td>ta</td><td>ta</td>
<td>cn</td><td>kO</td><td></td><td>r-</td><td></td>
<img file="LT3295B_D0020.tif" />
ti
S
TJ
<td> 33</td><td> 33</td><td>X</td><td>X</td>
<td>CM</td><td>CM</td><td>CM</td><td>CM</td>
<td>ta</td><td>ta</td><td>ta</td><td>ta</td>
<td>co</td><td>co</td><td>cn</td><td>cn</td>
<td>'O—*’</td><td> *—</td><td>ta—·</td><td>ta—</td>
<td>n</td><td>co</td><td>o</td><td>CO</td>
<td>m</td><td>LD</td><td>LO</td><td>LO</td>
<td>ta</td><td>ta</td><td>ta</td><td>ta</td>
<td>kO</td><td>kO</td><td>kO</td><td>kO</td>
<td>ta</td><td>ta</td><td>ta</td><td>ta</td>
<td></td><td>-—ta.</td><td></td><td>-—ta</td>
<td>K</td><td>K</td><td>K</td><td>X</td>
<td></td><td></td><td></td><td></td>
<td></td><td>ta</td><td>ta</td><td>ta</td>
<td>e</td><td>e</td><td>e</td><td>e</td>
<td> —</td><td>ta-*·</td><td>ta—-</td><td>ta—«'</td>
<td>cn</td><td>co</td><td>m</td><td>m</td>
<td>T~d</td><td>τ—-1</td><td>r~d</td><td>r-1</td>
<td>ta</td><td>ta</td><td>ta</td><td>ta</td>
<td> |</td><td>I</td><td> |</td><td>I</td>
<td>lo</td><td>1 O</td><td>1 O</td><td> 1</td>
<td> 00</td><td> 00</td><td>σ»</td><td>σ</td>
<td>ta</td><td>ta</td><td>ta</td><td>ta</td>
<td>co</td><td>co</td><td>co</td><td>co</td>
CM
I
CO (0
Ά
C
Φ
H
X
X
CM m
m m
ta
LO
CM
LO m
K
LO
X
CM
CM
O o
m >1
G
-A (0 a>
+4
CO •φ i—I Φ 44 G Φ ti
LT)
<td colspan="2">ro 1</td><td colspan="4">cn</td>
<td>to</td><td></td><td></td><td></td><td></td><td>f cn</td>
<td>(ti</td><td></td><td>cn</td><td>x</td><td></td><td></td>
<td>i—1</td><td></td><td> 1</td><td> 1</td><td></td><td>rH</td>
<td>•A</td><td></td><td>co</td><td>co</td><td></td><td>•rd</td>
<td>G</td><td></td><td>(ti</td><td>(ti</td><td></td><td>G</td>
<td> <3</td><td></td><td>rA</td><td>i—(</td><td></td><td> (3</td>
<td>A</td><td></td><td>•A</td><td>A</td><td></td><td>A</td>
<td>•A</td><td></td><td>C</td><td rowspan="2">S</td><td></td><td>•rd</td>
<td>ft</td><td> 1</td><td>!3 i</td><td> 1</td><td>ft</td>
<td>O A</td><td>Ί</td><td>A •A |</td><td>A •A</td><td>Ί</td><td>0 •rd</td>
<td> 44</td><td></td><td>ft</td><td>ft</td><td></td><td>X</td>
<td> 0</td><td></td><td> 0</td><td> 0</td><td></td><td>o</td>
<td>A</td><td></td><td>A</td><td>A</td><td></td><td>A</td>
<td>Ό</td><td></td><td>Ό</td><td>Τ3</td><td></td><td>ū</td>
<td>•H X</td><td></td><td>Ή X</td><td>•rd X</td><td></td><td>•rd X</td>
<td>(3 A</td><td></td><td>c3 A</td><td>(3 A</td><td></td><td>(3 A</td>
<td> 44</td><td></td><td>X</td><td>X</td><td></td><td>X</td>
<td>Φ</td><td></td><td>Φ</td><td>Φ</td><td></td><td>Φ</td>
<td> 44</td><td></td><td>X</td><td>X</td><td></td><td>X</td>
tetrahidropiranilas-3 - 3, 93 (m, 2H), 4,10 (m, 2H), 6, 53 (d, ĮH)
6,70 (d, IH)
<td colspan="2">CO</td><td>co</td><td colspan="2">co</td><td colspan="2">CO</td><td colspan="3">CO</td>
<td>(ti</td><td></td><td>(Ū</td><td></td><td>(ti</td><td></td><td> (0</td><td></td><td> (0</td><td></td>
<td>r—H</td><td>co</td><td>X</td><td>co</td><td>X</td><td>CO</td><td>i—(</td><td>CO</td><td> *—1</td><td>co</td>
<td>•rd</td><td> (0</td><td>-A</td><td>(ti</td><td>•A</td><td> (0</td><td>•A</td><td>(ti</td><td>X</td><td> (0</td>
<td>ft</td><td>l—(</td><td>ft</td><td>i—1</td><td>ft</td><td>i—1</td><td>ft</td><td>i—(</td><td>ft</td><td>X</td>
<td> 0</td><td>•A</td><td>O</td><td>-A</td><td> 0</td><td>A</td><td> 0</td><td>•A</td><td>o</td><td>X</td>
<td>A</td><td>X</td><td>A</td><td>X</td><td>A</td><td>X</td><td>A</td><td>X</td><td>A</td><td>X</td>
<td>ft</td><td>Φ</td><td>ft</td><td>Φ</td><td>ft</td><td>Φ</td><td>ft</td><td>Φ</td><td>ft</td><td>Φ</td>
<td>LO</td><td>r-</td><td> 03</td><td>σ</td><td>O</td><td>rA</td><td>CM</td><td>cn</td><td>x</td><td>ir></td>
<td>r“d</td><td>τ—1</td><td>t—1</td><td> 1—(</td><td>CM</td><td>CM</td><td>CM</td><td>CM</td><td>CM</td><td>CM</td>
e «3
Ή
-H
N (N
Ck
K r—I ta.
X a
tH ta
X
X tH ta
X
<td colspan="2">CO</td><td colspan="2">ta</td><td colspan="2">ta</td><td>O</td><td colspan="8">o</td>
<td>m</td><td></td><td></td><td></td><td></td><td></td><td>r-</td><td></td><td>z-ta</td><td>z-ta</td><td></td><td>z*ta</td><td></td><td></td><td></td>
<td>ta</td><td></td><td>a</td><td></td><td>a</td><td></td><td>ta</td><td>ta</td><td>a</td><td>a</td><td>a</td><td>a</td><td></td><td></td><td></td>
<td>LD</td><td></td><td>tH</td><td></td><td>tH</td><td></td><td>LO</td><td>LO</td><td>CM</td><td>CM</td><td>CM</td><td>CM</td><td></td><td></td><td></td>
<td></td><td></td><td>ta</td><td></td><td>ta</td><td></td><td></td><td></td><td>ta</td><td>ta</td><td>ta</td><td>ta</td><td></td><td></td><td></td>
<td></td><td></td><td>X</td><td></td><td>X</td><td></td><td>ta</td><td>ta</td><td> 0)</td><td> «</td><td>cn</td><td>cn</td><td></td><td></td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>z-></td><td> *—*·</td><td></td><td></td><td> **—*</td><td>Z-M.</td><td>z—ta</td><td></td>
<td>a</td><td></td><td>co</td><td></td><td>co</td><td></td><td>a</td><td>a</td><td>o</td><td>o</td><td>o</td><td>o</td><td>a</td><td>a</td><td></td>
<td>CM</td><td></td><td>UO</td><td></td><td>m</td><td></td><td>tH</td><td>tH</td><td>kO</td><td>LO</td><td>LO</td><td>LO</td><td>CM</td><td>CM</td><td></td>
<td></td><td></td><td></td><td></td><td>ta</td><td></td><td>ta</td><td>ta</td><td>ta</td><td>ta</td><td>ta</td><td>ta</td><td>ta</td><td>ta</td><td></td>
<td>r</td><td></td><td>LO</td><td></td><td>LO</td><td></td><td>X</td><td>X</td><td>LO</td><td>LO</td><td>LD</td><td>LO</td><td>m</td><td>cn</td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td>-ta—·</td><td>M-M</td><td></td><td></td><td></td><td></td><td>M—*</td><td>'MM’</td><td></td>
<td>O-</td><td></td><td>ta</td><td></td><td>ta.</td><td></td><td>co</td><td>CO</td><td>ta</td><td>ta</td><td>ta</td><td>ta</td><td>o</td><td>O</td><td></td>
<td>tH</td><td></td><td>Z-.</td><td></td><td></td><td></td><td>LC</td><td>uo</td><td></td><td>zzta.</td><td>Z—ta</td><td></td><td>LO</td><td>LO</td><td></td>
<td>ta</td><td></td><td>a</td><td></td><td>a</td><td></td><td></td><td>ta</td><td>a</td><td>a</td><td>a</td><td>a</td><td>ta.</td><td>ta</td><td></td>
<td>M<sup>1</sup></td><td></td><td></td><td></td><td>’T</td><td></td><td>kO</td><td>kO</td><td>M*</td><td></td><td></td><td>X</td><td>LD</td><td>LO</td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>ta</td><td>ta</td><td>ta</td><td></td><td></td><td></td>
<td>ta.</td><td></td><td>ε</td><td></td><td>ε</td><td></td><td>ta</td><td>ta</td><td>ε</td><td>ε</td><td>ε</td><td>H</td><td>ta</td><td>ta.</td><td></td>
<td>z-m.</td><td></td><td></td><td></td><td></td><td></td><td>z*ta</td><td>z-M</td><td></td><td> ·*—*</td><td></td><td>'MM’</td><td>z—ta</td><td>z-m.</td><td></td>
<td>a</td><td>a</td><td>O</td><td>a</td><td>O</td><td>a</td><td>a</td><td>a</td><td><Π</td><td>σι</td><td>σι</td><td>cn</td><td>a</td><td>a</td><td></td>
<td>CM</td><td>tH</td><td>tH</td><td>iH</td><td>tH</td><td>iH</td><td>CM</td><td>CM</td><td>o</td><td>o</td><td>o</td><td>o</td><td>CM</td><td>CM</td><td></td>
<td>ta.</td><td>ta</td><td>ta</td><td></td><td>ta</td><td>ta</td><td>ta</td><td>ta</td><td>ta</td><td>ta</td><td>ta</td><td>ta</td><td>ta</td><td>ta.</td><td></td>
<td>R</td><td>X</td><td>kt</td><td>X</td><td>X</td><td>X</td><td>ε</td><td>ε</td><td>X</td><td>X</td><td>’T</td><td></td><td>ε</td><td>ε</td><td></td>
<td></td><td></td><td>l</td><td> -—·»</td><td> 1</td><td></td><td></td><td></td><td> 1</td><td> 1</td><td> 1</td><td> 1</td><td></td><td> *—*</td><td>kO</td>
<td>co</td><td>o</td><td>o</td><td>o</td><td>o</td><td>o</td><td>o</td><td>o</td><td>o</td><td>o</td><td>co</td><td>co</td><td>CO</td><td>co</td><td>LO</td>
<td>σι</td><td>x</td><td>σι</td><td>x</td><td>σι</td><td>x</td><td>tH</td><td>tH</td><td> 00</td><td> 00</td><td>σ</td><td>σι</td><td>o</td><td>o</td><td> 1</td>
<td></td><td>ta</td><td>ta</td><td>ta</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>ta.</td><td></td>
<td>co</td><td>LO</td><td>co</td><td>kO</td><td>co</td><td>LO</td><td></td><td></td><td>co</td><td>co</td><td>co</td><td>co</td><td></td><td></td><td>LO</td>
lentelės tęsinys
CM
I
<td colspan="7">CM</td><td>cn</td>
<td></td><td></td><td></td><td></td><td> 1</td><td></td><td></td><td>(fl</td>
<td></td><td></td><td></td><td></td><td>cn</td><td></td><td></td><td>i—1</td>
<td></td><td></td><td></td><td></td><td> (0</td><td></td><td></td><td>-G</td>
<td></td><td></td><td></td><td></td><td>rH</td><td></td><td></td><td>fX</td>
<td> 1</td><td> 1</td><td> 1</td><td> 1 1</td><td>G J</td><td> 1 1</td><td> 1 1</td><td>o G</td>
<td>Ί</td><td>=i</td><td>Ί</td><td>Ί Ί</td><td>Φ Ί Ή</td><td>T T</td><td>Ί <sup>s</sup>i</td><td>-G a</td>
<td></td><td></td><td></td><td></td><td>X</td><td></td><td></td><td>i—1</td>
<td></td><td></td><td></td><td></td><td>rH</td><td></td><td></td><td>-G</td>
<td></td><td></td><td></td><td></td><td>•H</td><td></td><td></td><td>X</td>
<td></td><td></td><td></td><td></td><td>X</td><td></td><td></td><td>φ</td>
<td></td><td></td><td></td><td></td><td>Φ i</td><td></td><td></td><td>ε I</td>
<td></td><td></td><td></td><td></td><td>LD</td><td></td><td></td><td>1 tH</td>
<td></td><td></td><td></td><td>CO</td><td></td><td></td><td>co |</td><td></td>
<td></td><td></td><td></td><td>1 cn</td><td></td><td></td><td>1 cn</td><td></td>
<td></td><td>X</td><td></td><td>(fl</td><td>CO</td><td>X</td><td> <0</td><td>co</td>
<td></td><td> 1</td><td></td><td>X</td><td> 1</td><td> 1</td><td>i—(</td><td> 1</td>
<td></td><td>cn</td><td></td><td>•G</td><td>cn</td><td>cn</td><td>X</td><td>cn</td>
<td></td><td>te</td><td></td><td>C</td><td>cū</td><td> <0</td><td>G</td><td>(fl</td>
<td></td><td>i—t</td><td></td><td>(fl</td><td>rG</td><td>X</td><td> !3</td><td>i—1</td>
<td></td><td>•G</td><td></td><td>G</td><td>-G</td><td>-G</td><td>G</td><td>•G</td>
<td></td><td rowspan="2"> <3</td><td></td><td>-G</td><td>q</td><td>C</td><td>•G</td><td>C</td>
<td> 1</td><td> 1</td><td>a i</td><td>(3 i</td><td>?3 i</td><td>a i</td><td> <3</td>
<td>“l</td><td>G •G</td><td>Ί</td><td>O E •G 1</td><td>G E •G 1</td><td>G E •G |</td><td>O s X 1</td><td>G •G</td>
<td></td><td>a</td><td></td><td>X</td><td>a</td><td>a</td><td>X</td><td>a</td>
<td></td><td>o</td><td></td><td>o</td><td>o</td><td>o</td><td>o</td><td>o</td>
<td></td><td>G</td><td></td><td>G</td><td>G</td><td>G</td><td>G</td><td>G</td>
<td></td><td>X</td><td></td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td>
<td></td><td>•G</td><td></td><td>•H</td><td>•H</td><td>•H</td><td>•H</td><td>•G</td>
<td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td>
<td></td><td>G</td><td></td><td>G</td><td>G</td><td>G</td><td>G</td><td>G</td>
<td></td><td>X</td><td></td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td>
<td></td><td>Φ</td><td></td><td>Φ</td><td>Φ</td><td>Φ</td><td>Φ</td><td>Φ</td>
<td></td><td>X</td><td></td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td>
<td>cn</td><td colspan="2">cn</td><td colspan="3">cn</td><td colspan="2">on</td><td>cn</td><td colspan="3"> «</td>
<td>(fl</td><td></td><td>(fl</td><td></td><td>(fl</td><td></td><td> (0</td><td></td><td>cfl</td><td></td><td>(fl</td><td></td>
<td>i—1</td><td>cn</td><td>X</td><td>cn</td><td>»H</td><td>cn</td><td>i—(</td><td>cn</td><td>i—1</td><td>cn</td><td> <—(</td><td>cn</td>
<td>-G</td><td>(fl</td><td>•G</td><td> (0</td><td>•H</td><td>(fl</td><td>-G</td><td> <0</td><td>•G</td><td>(fl</td><td>•G</td><td>(fl</td>
<td>a</td><td>i—1</td><td>a</td><td>X</td><td>a</td><td>X</td><td>a</td><td>X</td><td>a</td><td> <—1</td><td>a</td><td>t—)</td>
<td>o</td><td>•G</td><td> 0</td><td>•G</td><td> 0</td><td>•G</td><td> 0</td><td>•G</td><td>o</td><td>•G</td><td> 0</td><td>G</td>
<td>G</td><td>X</td><td>G</td><td>X</td><td>G</td><td>X</td><td>G</td><td>X</td><td>G</td><td>X</td><td>G</td><td>X</td>
<td>a</td><td>Φ</td><td>a</td><td>Φ</td><td>a</td><td>Φ</td><td>a</td><td>Φ</td><td>a</td><td>Φ</td><td>a</td><td>Φ</td>
<td>LO</td><td>X</td><td> 00</td><td>σι</td><td>o</td><td>X</td><td>CM</td><td>X</td><td></td><td>UO</td><td>LO</td><td>X</td>
<td>CM</td><td>CM</td><td>CM</td><td>CM</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td>
i rp
T3 ė
-s <d •P •P
N •P
MP m
>1
C •r-l co
Φ·
-P co •Φ i—I Φ -P c
Φ r-
<td colspan="2">k</td><td colspan="3">k</td><td colspan="2">k</td><td colspan="2">k</td>
<td>z—k</td><td></td><td></td><td></td><td></td><td>z«k</td><td></td><td>Z—k</td><td></td>
<td>X</td><td></td><td></td><td>X</td><td></td><td>X</td><td></td><td>X</td><td></td>
<td>P</td><td></td><td></td><td>rp</td><td></td><td>P</td><td></td><td>«Ρ</td><td></td>
<td>k</td><td></td><td></td><td>k</td><td></td><td>k</td><td></td><td>k</td><td></td>
<td>ε</td><td></td><td></td><td>ε</td><td></td><td>ε</td><td></td><td>£į</td><td></td>
<td>kz</td><td></td><td></td><td>k-z</td><td></td><td>*k—T</td><td></td><td></td><td></td>
<td>Γ-</td><td></td><td></td><td>Γ-</td><td></td><td>ro</td><td></td><td>ro</td><td></td>
<td>ΟΟ</td><td></td><td></td><td>ΟΟ</td><td></td><td>o</td><td></td><td>o</td><td></td>
<td>k</td><td></td><td></td><td>k</td><td></td><td>k</td><td></td><td>k</td><td></td>
<td>m</td><td></td><td></td><td>ro</td><td></td><td> 90</td><td></td><td>LO</td><td></td>
<td></td><td></td><td></td><td>k</td><td></td><td>k</td><td></td><td>k</td><td></td>
<td>Z—k</td><td></td><td></td><td>zk.</td><td></td><td>Zk</td><td></td><td>Zk</td><td></td>
<td>X</td><td></td><td></td><td>X</td><td></td><td> 32</td><td></td><td>X</td><td></td>
<td>CM</td><td>X</td><td></td><td>CM</td><td>X</td><td>P</td><td></td><td>tP</td><td></td>
<td>k -P</td><td>P</td><td></td><td>X</td><td>P</td><td>k 3</td><td></td><td>k £</td><td></td>
<td></td><td>k</td><td></td><td>k™z</td><td></td><td></td><td></td><td></td><td></td>
<td>CTi</td><td>^ε</td><td></td><td>Ch</td><td> 3</td><td>Γ-</td><td></td><td>Γ-</td><td></td>
<td>o</td><td>ro</td><td></td><td>o</td><td>ro</td><td>ΟΟ</td><td></td><td>ΟΟ</td><td></td>
<td> <31</td><td>tn</td><td></td><td>k 'T</td><td>ro</td><td>LO</td><td></td><td>ro</td><td></td>
<td></td><td>LD</td><td></td><td></td><td>L0</td><td></td><td></td><td></td><td></td>
<td></td><td>k</td><td></td><td>k</td><td>k</td><td>k</td><td></td><td>k</td><td></td>
<td></td><td>Z—k</td><td></td><td>Zk</td><td>z«k</td><td>k</td><td>Z—k</td><td>z—k</td><td>Z«k</td>
<td>X</td><td>X</td><td></td><td>CM</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td>
<td>CM</td><td>P</td><td></td><td>CM</td><td>iP</td><td>CM</td><td>P</td><td>CM</td><td>rP</td>
<td>k</td><td>k</td><td></td><td>k</td><td>k,</td><td>k</td><td>k</td><td>k</td><td>k</td>
<td>ε</td><td>ε</td><td></td><td>ε</td><td>ε</td><td> 4-1</td><td>ε</td><td> 4-1</td><td>ε</td>
<td>z</td><td>’k-r</td><td>KT</td><td>k—'</td><td> *</td><td>k—*</td><td>k_z</td><td>kZ</td><td>kZ</td>
<td>o</td><td>PO</td><td> 00</td><td>o</td><td>ro</td><td>Ch</td><td>CO</td><td>Ch</td><td>CO</td>
<td>ch</td><td>o</td><td></td><td>o</td><td>o</td><td>o</td><td>LO</td><td>o</td><td>LT)</td>
<td>k</td><td>k</td><td>CM</td><td>k</td><td>k</td><td>k</td><td>k</td><td>k</td><td>k</td>
<td>ro</td><td>LO</td><td>CO</td><td>«Τ</td><td>LO</td><td></td><td> 90</td><td></td><td>LO</td>
I II I I ϊ <sup>=</sup>ι Ί Ί Ί co (d •H
Om
O
P a
ro r-
<td colspan="2"></td><td colspan="2">ro 1 co</td>
<td>’T</td><td></td><td>(d</td><td></td>
<td> 1</td><td></td><td>t—4</td><td></td>
<td>co</td><td></td><td>•H</td><td></td>
<td><d</td><td></td><td>C</td><td></td>
<td> '—1</td><td></td><td>id</td><td></td>
<td>•P</td><td></td><td>P</td><td></td>
<td>c</td><td></td><td>-P</td><td></td>
<td>(d</td><td> 1</td><td>a</td><td> 1</td>
<td>P •H</td><td>Ί</td><td>0 •P</td><td>Ί</td>
<td>a</td><td></td><td> 4-1</td><td></td>
<td>o</td><td></td><td>o</td><td></td>
<td>P</td><td></td><td>P</td><td></td>
<td>ro</td><td></td><td>X)</td><td></td>
<td>•P</td><td></td><td>•P</td><td></td>
<td>X</td><td></td><td>X</td><td></td>
<td>id</td><td></td><td>id</td><td></td>
<td>P</td><td></td><td>P</td><td></td>
<td> 4-></td><td></td><td>X</td><td></td>
<td>Φ</td><td></td><td>Φ</td><td></td>
<td> 4-1</td><td></td><td>X</td><td></td>
<td>w</td><td>CA d rp</td><td>co</td><td>co id i—1</td>
<td><u</td><td>•P</td><td>(d</td><td>P</td>
<td>P</td><td></td><td>P</td><td>a</td>
<td>•P</td><td>O</td><td>•P</td><td>o</td>
<td>-P</td><td>P</td><td>X</td><td>P</td>
<td>Q></td><td>Oi</td><td>Φ</td><td>a</td>
<td>ΟΊ</td><td>O</td><td>P</td><td>CM</td>
<td> 00</td><td></td><td>ST</td><td>•*r</td>
<td> •</td><td> •</td><td>k</td><td> •</td>
<td>r-</td><td>r-</td><td>r-</td><td>r-</td>
<td colspan="2"></td><td>a i—1</td><td colspan="3">a r-4</td><td colspan="2">a i—1</td>
<td></td><td></td><td></td><td></td><td>K</td><td></td><td></td><td></td>
<td></td><td></td><td>Ό</td><td></td><td>Ό</td><td></td><td>τ)</td><td></td>
<td></td><td></td><td> ****</td><td></td><td></td><td></td><td> ·*—*</td><td></td>
<td></td><td></td><td>n</td><td></td><td>co</td><td></td><td>co</td><td></td>
<td></td><td></td><td>co</td><td></td><td>co</td><td></td><td>co</td><td></td>
<td>a</td><td></td><td> *»</td><td></td><td>K</td><td></td><td></td><td></td>
<td>Ν’</td><td></td><td>Ό</td><td></td><td>kO</td><td></td><td>kO</td><td></td>
<td>e</td><td></td><td></td><td></td><td> ·»</td><td></td><td> ·»</td><td></td>
<td></td><td></td><td></td><td>a</td><td></td><td></td><td> >-></td><td>a</td>
<td>CM</td><td></td><td>X</td><td>CM</td><td>□C</td><td>Λ</td><td>te</td><td>CM</td>
<td>Ν'</td><td></td><td>r-1</td><td>K</td><td>i—1</td><td>CM</td><td>i—1</td><td></td>
<td></td><td></td><td></td><td> 3</td><td>v</td><td></td><td>K</td><td>s</td>
<td>co</td><td></td><td>ε.</td><td></td><td>ε.</td><td>Ό</td><td>ε.</td><td></td>
<td> 1</td><td></td><td></td><td>o</td><td></td><td> ·—*</td><td></td><td>o</td>
<td>o</td><td></td><td>CM</td><td>Ν'</td><td>CM</td><td>o</td><td>CM</td><td>N*</td>
<td>o</td><td></td><td></td><td></td><td>cn</td><td></td><td>σ</td><td></td>
<td></td><td></td><td>K</td><td>r-</td><td>V</td><td>K</td><td>K</td><td>Γ'</td>
<td><O</td><td></td><td>cf)</td><td></td><td>m</td><td>r*</td><td>tn</td><td></td>
<td></td><td></td><td></td><td> >.</td><td></td><td></td><td></td><td>t.</td>
<td>k.</td><td>a</td><td></td><td></td><td> *»</td><td></td><td>s</td><td></td>
<td></td><td>rP</td><td></td><td>a</td><td></td><td></td><td></td><td>a</td>
<td>a</td><td> %</td><td>a</td><td>Tp</td><td>a</td><td>te</td><td>a</td><td>i—l</td>
<td>CM</td><td>ff)</td><td>CM</td><td></td><td>CM</td><td> 1—1</td><td>CM</td><td>K</td>
<td></td><td>i—1</td><td></td><td>w</td><td></td><td></td><td>K</td><td>n</td>
<td>-P</td><td>O.</td><td>P</td><td> £</td><td>ε</td><td>w</td><td>P</td><td>Λ</td>
<td> <-*·</td><td></td><td> ·*—*</td><td></td><td>*—P</td><td></td><td></td><td></td>
<td>CO</td><td>co</td><td>co</td><td>m</td><td>m</td><td>LT)</td><td>co</td><td>in</td>
<td>i—1</td><td>m</td><td>i—1</td><td>tn</td><td>i—1</td><td>tn</td><td>r-4</td><td>tn</td>
<td>K</td><td></td><td></td><td>K</td><td>χ</td><td>K</td><td></td><td> *.</td>
<td></td><td></td><td></td><td>co</td><td></td><td>kO</td><td></td><td>co</td>
tiO-CH<sub>2</sub>C^<sub>2</sub>CH-CH~W
<img file="LT3295B_D0021.tif" />
co
8.05 etilas tetrahidropiranilas-3 tienilas-2 4,15(t,2H), 6, 00(dt,lH), 6,60(d,1H)
6, 90 (m, 2H), 7,10 (d, 1H)
Nr. R<sub>x</sub> R<sub>2</sub> W fizikiniai duomenys: BMR: m. d. lyd.
<td colspan="2">k</td><td colspan="2"></td><td colspan="2">k</td><td colspan="2"></td><td colspan="2">k</td><td colspan="6">k</td>
<td>k</td><td></td><td>^-k</td><td></td><td>*»-k</td><td></td><td>k</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td>
<td> 33</td><td></td><td> 35</td><td></td><td> 35</td><td></td><td> 35</td><td></td><td> 35</td><td></td><td> 35</td><td></td><td></td><td></td><td></td><td></td>
<td>rH</td><td></td><td>rH</td><td></td><td>rH</td><td></td><td>tp</td><td></td><td>rH</td><td></td><td>ip</td><td></td><td></td><td></td><td></td><td></td>
<td>k</td><td></td><td>k</td><td></td><td>k</td><td></td><td>k</td><td></td><td>k</td><td></td><td>k</td><td></td><td></td><td></td><td></td><td></td>
<td>Ό</td><td></td><td>TJ</td><td></td><td>T)</td><td></td><td>TJ</td><td></td><td>TJ</td><td></td><td>TJ</td><td></td><td></td><td></td><td></td><td></td>
<td>k—*</td><td></td><td>'k-*</td><td></td><td>k-»</td><td></td><td>k-z</td><td></td><td>k—*</td><td></td><td>kz</td><td></td><td> 1</td><td></td><td> 1</td><td></td>
<td>o</td><td></td><td>O</td><td></td><td>o</td><td></td><td>o</td><td></td><td>o</td><td></td><td>o</td><td></td><td></td><td></td><td>Γ-</td><td></td>
<td>co</td><td></td><td>LO</td><td></td><td>LO</td><td></td><td>co</td><td></td><td>CD</td><td></td><td>LO</td><td></td><td>co</td><td></td><td>ΟΟ</td><td></td>
<td>k</td><td></td><td>k</td><td></td><td>k</td><td></td><td>k</td><td></td><td>k</td><td></td><td>k</td><td></td><td>k</td><td></td><td>k</td><td></td>
<td>co</td><td></td><td>co</td><td></td><td>co</td><td></td><td>co</td><td></td><td>co</td><td></td><td>co</td><td></td><td>co</td><td></td><td>co</td><td></td>
<td></td><td></td><td>k</td><td></td><td>k</td><td></td><td>k</td><td></td><td>k</td><td></td><td>k</td><td></td><td>k</td><td></td><td>k</td><td></td>
<td></td><td></td><td>k</td><td></td><td>K</td><td></td><td>χ-k.</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>^k,</td><td></td>
<td> 33</td><td></td><td> 35</td><td></td><td> 35</td><td></td><td> 35</td><td></td><td> 35</td><td></td><td> 33</td><td></td><td> 33</td><td></td><td> 33</td><td></td>
<td>rH</td><td></td><td>rH</td><td></td><td>rH</td><td></td><td>rH</td><td></td><td>rH</td><td></td><td>rH</td><td></td><td>tP</td><td></td><td>rH</td><td></td>
<td>k</td><td></td><td>k</td><td></td><td>k</td><td></td><td>k</td><td></td><td>k</td><td></td><td>k</td><td></td><td>k</td><td></td><td>k</td><td></td>
<td> +-></td><td></td><td> 4-></td><td></td><td> 4-></td><td></td><td> 4-1</td><td></td><td>-P</td><td></td><td> 4-1</td><td></td><td>4-t</td><td></td><td>4-t</td><td></td>
<td>TJ</td><td></td><td>TJ</td><td></td><td>TJ</td><td></td><td>TJ</td><td></td><td>s</td><td></td><td>TJ</td><td></td><td>S</td><td></td><td>TJ</td><td></td>
<td></td><td></td><td>k-*</td><td></td><td>’kr’</td><td></td><td></td><td></td><td></td><td></td><td>k»·»</td><td></td><td></td><td></td><td>k-r</td><td></td>
<td>o</td><td></td><td>O</td><td></td><td>O</td><td></td><td>O</td><td></td><td>o</td><td></td><td>o</td><td></td><td>Γ-</td><td></td><td>Γ-</td><td></td>
<td>o</td><td>k</td><td>o</td><td>k</td><td>o</td><td>^-k</td><td>o</td><td></td><td>o</td><td></td><td>tp</td><td>,^-k</td><td>ΟΟ</td><td></td><td>ΟΟ</td><td></td>
<td>k</td><td>X</td><td>k</td><td> 32</td><td>k</td><td> 32</td><td>k</td><td>X</td><td></td><td>X</td><td>k</td><td> 33</td><td></td><td></td><td>k</td><td></td>
<td>co</td><td>co</td><td>LO</td><td>co</td><td>co</td><td>co</td><td>LO</td><td>co</td><td>LO</td><td>co</td><td>LO</td><td> 147</td><td> 147</td><td></td><td> 147</td><td></td>
<td></td><td></td><td></td><td>K.</td><td></td><td>k</td><td></td><td>k</td><td></td><td>k</td><td></td><td>k</td><td></td><td></td><td></td><td></td>
<td>k</td><td> £</td><td>k</td><td> £</td><td>k</td><td> £</td><td>k</td><td> £</td><td>k</td><td> _£</td><td>k</td><td>o.</td><td>k</td><td></td><td>k</td><td></td>
<td>^—k</td><td></td><td>k</td><td>'k*'</td><td>x-k</td><td></td><td>k</td><td>k-*</td><td></td><td></td><td></td><td></td><td>^-k</td><td>k</td><td>k</td><td>y—k</td>
<td> 35</td><td>o</td><td> 32</td><td>O</td><td> 35</td><td>O</td><td> 35</td><td>o</td><td> 32</td><td>o</td><td> 32</td><td>o</td><td> 33</td><td> 33</td><td> 33</td><td> 33</td>
<td>CM</td><td>CM</td><td>CM</td><td>CM</td><td>CM</td><td>CM</td><td>CM</td><td>CM</td><td>CM</td><td> 07</td><td>CM</td><td>CM</td><td>CM</td><td> 07</td><td>CM</td><td> 07</td>
<td>k</td><td>k</td><td>k</td><td>k</td><td>k</td><td>k</td><td>k</td><td>k</td><td>k</td><td>k</td><td>k</td><td>k</td><td>k</td><td>k</td><td>k</td><td>k</td>
<td> 4-></td><td>r-</td><td>-P</td><td>r—</td><td> 4-></td><td>r-</td><td>4J</td><td>r-</td><td> 4-></td><td>r-</td><td>-P</td><td>r*</td><td> 4-></td><td> £^</td><td> 4-1</td><td> 3</td>
<td>k—’</td><td> 1</td><td>k*·</td><td> |</td><td></td><td> 1</td><td></td><td> 1</td><td>•k--</td><td> 1</td><td></td><td>l</td><td> >—·</td><td></td><td> ——*</td><td></td>
<td>o</td><td>o</td><td>LT)</td><td>O</td><td>v</td><td>o</td><td> 147</td><td>o</td><td> 147</td><td>o</td><td>o</td><td>o</td><td> 07</td><td> 07</td><td> 07</td><td> 07</td>
<td>T—1</td><td> 00</td><td>rH</td><td> 00</td><td>I—1</td><td> 00</td><td>i—1</td><td> 00</td><td> 1—1</td><td> 00</td><td>CM</td><td> 00</td><td>t-l</td><td>r-</td><td> ,—1</td><td>CO</td>
<td></td><td>k</td><td>k</td><td>k</td><td></td><td>k</td><td></td><td>k</td><td></td><td>k</td><td>k</td><td>k</td><td> —</td><td>k</td><td></td><td>k</td>
<td>ν’</td><td>LO</td><td></td><td>LO</td><td>v</td><td>LO</td><td>V</td><td>LO</td><td>ν’</td><td>co</td><td><T</td><td>LO</td><td>V</td><td>co</td><td>ν’</td><td>co</td>
<td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>CM I</td><td></td><td></td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>UI</td><td></td><td></td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>u</td><td></td><td></td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>i—1</td><td></td><td></td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>H</td><td></td><td></td><td></td>
<td>I</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>C</td><td></td><td></td><td></td>
<td> 1</td><td></td><td> 1</td><td></td><td> 1</td><td></td><td>CM</td><td></td><td> 1</td><td></td><td> 1</td><td></td><td>Φ</td><td></td><td> 1</td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td> 1</td><td></td><td></td><td></td><td></td><td></td><td>•H</td><td></td><td></td><td></td>
<td> 1</td><td></td><td> 1</td><td></td><td> 1</td><td></td><td>m</td><td></td><td> 1</td><td></td><td> 1</td><td></td><td> 4-1</td><td></td><td> 1</td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td>Φ</td><td></td><td></td><td></td><td></td><td></td><td>r—1</td><td></td><td></td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td>i—1</td><td></td><td></td><td></td><td></td><td></td><td>H</td><td></td><td></td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td>•H</td><td></td><td></td><td></td><td></td><td></td><td> 4-></td><td></td><td></td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td>C</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td>Φ</td><td></td><td></td><td></td><td></td><td></td><td>E</td><td></td><td></td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td>Ή</td><td></td><td></td><td></td><td></td><td></td><td> 1</td><td></td><td></td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td> 4-1</td><td></td><td></td><td></td><td></td><td></td><td>m</td><td></td><td></td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td>o7</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td>to</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td>u</td><td></td><td></td><td></td><td>UI</td><td></td><td>Ui</td><td></td><td></td><td></td>
<td></td><td></td><td> 1</td><td></td><td></td><td></td><td>Γ—1</td><td></td><td></td><td></td><td>(Ū</td><td></td><td> 1</td><td></td><td></td><td></td>
<td></td><td></td><td>co</td><td></td><td></td><td></td><td>•H</td><td></td><td></td><td></td><td>i—1</td><td></td><td>UI</td><td></td><td></td><td></td>
<td></td><td></td><td>Π3</td><td></td><td></td><td></td><td>C</td><td></td><td></td><td></td><td>•H</td><td></td><td> <0</td><td></td><td></td><td></td>
<td></td><td></td><td>rp</td><td></td><td></td><td></td><td>Φ</td><td></td><td></td><td></td><td>C</td><td></td><td>i—1</td><td></td><td></td><td></td>
<td></td><td></td><td>•H</td><td></td><td></td><td></td><td>t-l</td><td></td><td></td><td></td><td>Φ</td><td></td><td>H</td><td></td><td></td><td></td>
<td></td><td></td><td>C</td><td></td><td></td><td></td><td>H</td><td></td><td></td><td></td><td>M-l</td><td></td><td>G</td><td></td><td></td><td></td>
<td> 1</td><td></td><td>nJ</td><td></td><td> 1</td><td></td><td>a</td><td></td><td> 1</td><td></td><td>rp</td><td></td><td> <3</td><td></td><td> 1</td><td></td>
<td>Ί</td><td></td><td>P •H</td><td></td><td>Ί</td><td></td><td>o r4</td><td></td><td>Ί</td><td></td><td>•P 4-t</td><td></td><td>t-t •H</td><td></td><td>Ί</td><td></td>
<td></td><td></td><td>(X</td><td></td><td></td><td></td><td> 4-1</td><td></td><td></td><td></td><td></td><td></td><td>a</td><td></td><td></td><td></td>
<td></td><td></td><td> 0</td><td></td><td></td><td></td><td>O</td><td></td><td></td><td></td><td> $5</td><td></td><td>o</td><td></td><td></td><td></td>
<td></td><td></td><td>P</td><td></td><td></td><td></td><td>t-l</td><td></td><td></td><td></td><td>•P</td><td></td><td>t4</td><td></td><td></td><td></td>
<td></td><td></td><td>TJ</td><td></td><td></td><td></td><td>TJ</td><td></td><td></td><td></td><td> 14</td><td></td><td>•u</td><td></td><td></td><td></td>
<td></td><td></td><td>•P</td><td></td><td></td><td></td><td>•P</td><td></td><td></td><td></td><td> 4-></td><td></td><td>-H</td><td></td><td></td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>CO</td><td></td><td></td><td></td><td></td><td></td>
<td></td><td></td><td>J-l</td><td></td><td></td><td></td><td>t-l</td><td></td><td></td><td></td><td>k</td><td></td><td>t-l</td><td></td><td></td><td></td>
<td></td><td></td><td>4-t</td><td></td><td></td><td></td><td>4-t</td><td></td><td></td><td></td><td>ν’</td><td></td><td>4-t</td><td></td><td></td><td></td>
<td></td><td></td><td>Φ</td><td></td><td></td><td></td><td>Φ</td><td></td><td></td><td></td><td>k</td><td></td><td>Φ</td><td></td><td></td><td></td>
<td></td><td></td><td> 4-></td><td></td><td></td><td></td><td>4-t</td><td></td><td></td><td></td><td>CM</td><td></td><td>4-t</td><td></td><td></td><td></td>
<td>tn</td><td></td><td></td><td></td><td>U)</td><td></td><td></td><td></td><td>m</td><td></td><td></td><td></td><td></td><td></td><td>n</td><td></td>
<td>Φ</td><td></td><td></td><td></td><td> (0</td><td></td><td></td><td></td><td>Φ</td><td></td><td></td><td></td><td></td><td></td><td>u</td><td></td>
<td>ι—1</td><td></td><td>to</td><td></td><td>l—t</td><td></td><td>to</td><td></td><td> 1—1</td><td></td><td>UI</td><td></td><td>UI</td><td></td><td>i—1</td><td></td>
<td>Ή</td><td></td><td> (0</td><td></td><td>•H</td><td></td><td> (0</td><td></td><td>•H</td><td></td><td>U</td><td></td><td> (0</td><td></td><td>r4</td><td></td>
<td>a</td><td></td><td>r-H</td><td></td><td>a</td><td></td><td>rp</td><td></td><td>a</td><td></td><td> <—1</td><td></td><td>Γ—Ι</td><td></td><td>a</td><td></td>
<td> 0</td><td></td><td>•P</td><td></td><td> 0</td><td></td><td>•P</td><td></td><td> 0</td><td></td><td>H</td><td></td><td>Ή</td><td></td><td>o</td><td></td>
<td>n</td><td></td><td>-P</td><td></td><td>t-l</td><td></td><td> 4-></td><td></td><td>n</td><td></td><td>4-t</td><td></td><td> 4-1</td><td></td><td>t4</td><td></td>
<td>a</td><td></td><td>Φ</td><td></td><td>a</td><td></td><td>Φ</td><td></td><td>a</td><td></td><td>Φ</td><td></td><td>Φ</td><td></td><td>a</td><td></td>
<td>co</td><td></td><td></td><td></td><td>oo</td><td></td><td>σ</td><td></td><td>o</td><td></td><td>i—1</td><td></td><td>CM</td><td></td><td> 07</td><td></td>
<td>o</td><td></td><td>o</td><td></td><td>o</td><td></td><td>o</td><td></td><td>rH</td><td></td><td>l—1</td><td></td><td>r—1</td><td></td><td>iP</td><td></td>
<td> 00</td><td></td><td> 00</td><td></td><td>oo</td><td></td><td> 00</td><td></td><td> 00</td><td></td><td> 00</td><td></td><td> 00</td><td></td><td> 00</td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>x</td><td></td><td> «></td><td></td><td>X</td><td></td><td>X</td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>Χ-Χ</td><td></td><td>X—X</td><td></td><td>XX</td><td></td><td>Χ-Χ</td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>E</td><td></td><td>E</td><td></td><td>E</td><td></td><td>E</td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>τ—1</td><td></td><td>rd</td><td></td><td>rd</td><td></td><td>rd</td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>X</td><td></td><td>X</td><td></td><td>x</td><td></td><td>X</td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>Ό</td><td></td><td>Ό</td><td></td><td>x></td><td></td><td>τ)</td><td></td>
<td> |</td><td></td><td> |</td><td></td><td> 1</td><td></td><td> 1</td><td></td><td>X»*</td><td></td><td>X-r</td><td></td><td>χ-*’</td><td></td><td>•χ-»*</td><td></td>
<td>r*</td><td></td><td>Γ-</td><td></td><td>i^-</td><td></td><td>Γ-</td><td></td><td>co</td><td></td><td>co</td><td></td><td>O</td><td></td><td>o</td><td></td>
<td>m</td><td></td><td>ΓΟ</td><td></td><td>cn</td><td></td><td>όη</td><td></td><td>sr</td><td></td><td>sr</td><td></td><td>LO</td><td></td><td>co</td><td></td>
<td></td><td></td><td>X</td><td></td><td>X</td><td></td><td>X</td><td></td><td>X</td><td></td><td>χ</td><td></td><td>X</td><td></td><td>X</td><td></td>
<td>LO</td><td></td><td>LO</td><td></td><td>co</td><td></td><td>LO</td><td></td><td>LO</td><td></td><td>LO</td><td></td><td>co</td><td></td><td>co</td><td></td>
<td>x</td><td></td><td>x</td><td></td><td>X</td><td></td><td>x</td><td></td><td>h.</td><td></td><td>X</td><td></td><td>X</td><td></td><td>X</td><td></td>
<td></td><td></td><td></td><td></td><td>χβχ</td><td></td><td></td><td></td><td>^-χ</td><td>X</td><td>XX</td><td></td><td>XX</td><td></td><td>Χ-Χ</td><td></td>
<td>X</td><td></td><td>E</td><td></td><td>E</td><td></td><td>E</td><td></td><td>re</td><td>Χ-Χ</td><td>re</td><td>Χ-Χ</td><td>E</td><td></td><td>E</td><td></td>
<td>rd</td><td></td><td>ri</td><td></td><td>rd</td><td></td><td>rd</td><td></td><td>r-1</td><td>E</td><td>rd</td><td>re</td><td>rd</td><td></td><td>rd</td><td></td>
<td>x</td><td></td><td>X</td><td></td><td>x</td><td></td><td>X</td><td></td><td>X</td><td>r-1</td><td>X</td><td>rd</td><td>X</td><td></td><td>X</td><td></td>
<td>P</td><td></td><td>E</td><td></td><td>E</td><td></td><td>E</td><td></td><td>P</td><td>X</td><td>P</td><td>X</td><td>E</td><td></td><td>E</td><td></td>
<td></td><td></td><td>Ό</td><td></td><td>Ό</td><td></td><td>TJ</td><td></td><td>TJ</td><td>u</td><td>*Ū</td><td>Ό</td><td>Τ3</td><td></td><td>Ό</td><td></td>
<td></td><td></td><td>X-»·</td><td></td><td></td><td></td><td>Χ-*</td><td></td><td>X»'</td><td>X—··*</td><td>x-r</td><td>X-*</td><td>X»*</td><td></td><td>X-**</td><td></td>
<td>Γ-</td><td></td><td>Γ-</td><td></td><td>co</td><td></td><td> 00</td><td></td><td>cn</td><td>m</td><td>co</td><td>m</td><td>o</td><td></td><td>o</td><td></td>
<td>ΟΟ</td><td></td><td>ΟΟ</td><td></td><td> 00</td><td></td><td> 00</td><td></td><td>σ\</td><td>r-</td><td>a></td><td>r-</td><td>o</td><td>XX</td><td>o</td><td>χ—χ</td>
<td>X</td><td></td><td>X</td><td></td><td>X</td><td></td><td>x</td><td></td><td>x</td><td>x</td><td>X</td><td>X</td><td>χ</td><td>E</td><td>X</td><td>E</td>
<td>m</td><td></td><td>tn</td><td></td><td>LO</td><td></td><td>LO</td><td></td><td>LO</td><td>LO</td><td>cn</td><td>LO</td><td>LO</td><td>cn</td><td>LO</td><td>cn</td>
<td>x</td><td></td><td>X</td><td></td><td>X</td><td></td><td>X</td><td></td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>ε</td><td>X</td><td>ε</td>
<td>xx^</td><td>XX</td><td>χ—χ</td><td></td><td>,x«x</td><td>X—\</td><td>χ—χ</td><td>χ»>χ</td><td>XX</td><td>x*x</td><td>χ-X</td><td>χ>χ</td><td>X*X</td><td> —**</td><td>χ-β^</td><td>χ<sup>-</sup>*</td>
<td>E</td><td>E</td><td>E</td><td>X</td><td>E</td><td>re</td><td>te</td><td>re</td><td>E</td><td>re</td><td>E</td><td>E</td><td>re</td><td>o</td><td>E</td><td>O</td>
<td>CN</td><td>cn</td><td>CN</td><td>CO</td><td>CN</td><td>co</td><td>CM</td><td>co</td><td>CN</td><td>rd</td><td>CM</td><td>i—1</td><td>CM</td><td>CN</td><td>CN</td><td>co</td>
<td>X</td><td>X</td><td></td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td>
<td>E</td><td></td><td>E</td><td> 3</td><td>E</td><td></td><td>E</td><td>ε</td><td>E</td><td>TJ</td><td>E</td><td>Ί5</td><td>E</td><td>r-</td><td>E</td><td>r-</td>
<td></td><td></td><td>X—*</td><td></td><td> '-*'</td><td></td><td> *-*-</td><td>X--</td><td>X—'</td><td>X—·</td><td>Χ-*</td><td>Χ-*</td><td>χ-''</td><td> 1</td><td>X—·</td><td> 1</td>
<td>m</td><td>m</td><td>co</td><td>cn</td><td>co</td><td>m</td><td>co</td><td>co</td><td>LO</td><td>CO</td><td>cn</td><td>CO</td><td>cn</td><td>o</td><td>cn</td><td>o</td>
<td>rd</td><td>Γ'</td><td>rd</td><td>r</td><td>rd</td><td>Γ'</td><td>t—i</td><td>r-</td><td>rd</td><td>LO</td><td>rd</td><td>LO</td><td>rd</td><td> 00</td><td>rd</td><td> 00</td>
<td>x</td><td>X</td><td>x</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>x</td><td>χ</td>
<td>ST</td><td>LO</td><td>'T</td><td>co</td><td>sr</td><td>co</td><td>ST</td><td>LO</td><td>sr</td><td>LO</td><td></td><td>LO</td><td>sr</td><td>LO</td><td>sr</td><td>LO</td>
<img file="LT3295B_D0022.tif" />
<td colspan="3">(N</td>
<td>1 tn fl E -P C Φ</td><td> 1</td><td>CN</td>
<td>-P</td><td></td><td> 1</td>
<td>E</td><td> 1</td><td>tn</td>
<td>P</td><td></td><td>td</td>
<td>O</td><td></td><td>ι—1</td>
<td>i—1</td><td></td><td>•P</td>
<td>E</td><td></td><td>G</td>
<td>U</td><td></td><td>Φ</td>
<td> 1</td><td></td><td>-P</td>
<td>cn</td><td></td><td>E</td>
os n cn
I I tn tn tn >1
C
P tn ar
E tn
-Φ
E
Φ
E
G
Φ /E
OS
<td>sr 1</td><td colspan="2"><a rd</td><td colspan="2">cn 1</td><td>cn 1</td><td>(d E</td>
<td>tn</td><td></td><td>•rd</td><td></td><td>tn</td><td>cn</td><td>-P</td>
<td>td</td><td></td><td>G</td><td></td><td>td</td><td> <0</td><td>G</td>
<td> 1—1</td><td></td><td> 3</td><td></td><td>i-d</td><td>E</td><td> 3</td>
<td>-P</td><td></td><td>P</td><td></td><td>•H</td><td>•P</td><td>P</td>
<td>G</td><td></td><td>•td</td><td></td><td>c</td><td>C</td><td>-P</td>
<td> 3</td><td> 1</td><td>a</td><td> 1</td><td> 3</td><td> 3</td><td>a</td>
<td>p</td><td></td><td>o</td><td> —</td><td>P</td><td>P</td><td>o</td>
<td>-P</td><td>Ί</td><td>•rd</td><td>Ί</td><td>P</td><td>P</td><td>-P</td>
<td>a</td><td></td><td>E</td><td></td><td>a</td><td>a</td><td>E</td>
<td>o P</td><td></td><td>O P</td><td></td><td>o U</td><td>0 P</td><td>O U</td>
<td>•9 •P E</td><td></td><td>9 •H E</td><td></td><td>b ••d E</td><td>-9 •P E</td><td>•9 -P E</td>
<td>(3 P</td><td></td><td>«3 P</td><td></td><td><3 P</td><td>t3 P</td><td><3 P</td>
<td>E</td><td></td><td>E</td><td></td><td>E</td><td>E</td><td>E</td>
<td>Φ</td><td></td><td>Φ</td><td></td><td>Φ</td><td>Φ</td><td>Φ</td>
<td>E</td><td></td><td>E</td><td></td><td>E</td><td>E</td><td>E</td>
<td></td><td colspan="2">tn ta</td><td colspan="2">tn <a</td><td>cn td</td><td colspan="2">tn <a</td>
<td>tn</td><td>rd</td><td>tn</td><td>rd</td><td>tn</td><td>E</td><td>tn</td><td>r“d</td>
<td>n3</td><td>•rd</td><td>(d</td><td>•rd</td><td>ta</td><td>-P</td><td><d</td><td>•rd</td>
<td>r-d</td><td>a</td><td>E</td><td>a</td><td>rd</td><td>a</td><td>rd</td><td>a</td>
<td>•H</td><td>o</td><td>-P</td><td> 0</td><td>•rd</td><td> 0</td><td>•P</td><td> 0</td>
<td> 4-></td><td>P</td><td>E</td><td>P</td><td>-P</td><td>P</td><td>E</td><td>P</td>
<td>Φ</td><td>a</td><td>Φ</td><td>a</td><td>Φ</td><td>a</td><td>Φ</td><td>a</td>
<td>sr</td><td>LO</td><td>LO</td><td></td><td> 00</td><td>tn</td><td>σι</td><td>O</td>
<td>rd</td><td>rd</td><td>rd</td><td>rd</td><td>rd</td><td>E</td><td>o</td><td>rd</td>
<td>co</td><td>X 00</td><td> 00</td><td> 00</td><td> 00</td><td> 00</td><td>m</td><td> 00</td>
Nr. R<sub>l</sub> R<sub>2</sub> W fizikiniai duomenys: BMR: m. d. lyd.
<td colspan="2"></td><td colspan="14">ta</td>
<td>X</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td><Tta</td><td></td>
<td>X</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>X</td><td></td>
<td>f—d</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>rd</td><td></td>
<td>ta</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>ta</td><td></td>
<td>T)</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td> 3</td><td></td>
<td>-r’</td><td></td><td> 1</td><td></td><td> 1</td><td></td><td> 1</td><td></td><td> 1</td><td></td><td> 1</td><td></td><td> 1</td><td></td><td></td><td></td>
<td>o</td><td></td><td>Γ-</td><td></td><td>r—</td><td></td><td>r—</td><td></td><td>Γ—</td><td></td><td>r-</td><td></td><td>r-</td><td></td><td>MO</td><td></td>
<td>kO</td><td></td><td>ΓΟ</td><td></td><td>X</td><td></td><td>X</td><td></td><td>X</td><td></td><td>X</td><td></td><td>X</td><td></td><td>V</td><td></td>
<td>ta</td><td></td><td>ta</td><td></td><td>ta</td><td></td><td>ta</td><td></td><td>ta</td><td></td><td>ta</td><td></td><td>ta</td><td></td><td>ta</td><td></td>
<td>kO</td><td></td><td>MO</td><td></td><td>kO</td><td></td><td>kO</td><td></td><td>MO</td><td></td><td>MO</td><td></td><td>MO</td><td></td><td>kO</td><td></td>
<td>ta</td><td></td><td>X</td><td></td><td>ta</td><td></td><td>ta</td><td></td><td>ta</td><td></td><td>ta</td><td></td><td>ta</td><td></td><td>ta</td><td></td>
<td> *—»</td><td></td><td>*-ta</td><td></td><td></td><td></td><td>X.</td><td></td><td>,*-Χ,</td><td></td><td>^*Χχ,</td><td></td><td></td><td></td><td>*-ta</td><td></td>
<td>X</td><td></td><td>X</td><td></td><td>X</td><td></td><td>X</td><td></td><td>X</td><td></td><td>X</td><td></td><td>X</td><td></td><td>X</td><td>^*ta.</td>
<td>i-d</td><td></td><td>rd</td><td></td><td>rd</td><td></td><td>rd</td><td></td><td>rd</td><td></td><td>rd</td><td></td><td>rd</td><td></td><td>rd</td><td>X</td>
<td>ta</td><td></td><td>ta</td><td></td><td>ta</td><td></td><td>ta</td><td></td><td> ·»,</td><td></td><td>ta</td><td></td><td>ta</td><td></td><td>ta</td><td>rd</td>
<td>-P</td><td></td><td>-P</td><td></td><td>-P</td><td></td><td>-P</td><td></td><td> 4-1</td><td></td><td>-P</td><td></td><td>-P</td><td></td><td>-P</td><td>ta</td>
<td></td><td></td><td>TJ</td><td></td><td>Ό</td><td></td><td>Ό</td><td></td><td>Ό</td><td></td><td>τί</td><td></td><td></td><td></td><td>Ό</td><td>Ό</td>
<td></td><td></td><td></td><td></td><td> *>—·</td><td></td><td> ·»—*</td><td></td><td>ta*»</td><td></td><td>ta*»·</td><td></td><td>•«χ*»</td><td></td><td> —-»»</td><td>ta*»</td>
<td>o</td><td></td><td>Γ—</td><td></td><td>Γ-</td><td></td><td>Γ-</td><td></td><td>Γ-</td><td></td><td> 00</td><td></td><td> 00</td><td></td><td>co</td><td>tn</td>
<td>rd</td><td>^-x</td><td> 00</td><td></td><td>ΟΟ</td><td></td><td>ΟΟ</td><td></td><td>ΟΟ</td><td></td><td> 00</td><td></td><td>co</td><td></td><td>os</td><td>r-</td>
<td>ta</td><td>X</td><td>ta</td><td></td><td>ta</td><td></td><td>ta</td><td></td><td>ta</td><td></td><td>ta</td><td></td><td>ta</td><td></td><td>ta</td><td>κ</td>
<td>kO</td><td>to</td><td>m</td><td></td><td>X</td><td></td><td>LT)</td><td></td><td>LT)</td><td></td><td>LO</td><td></td><td>LO</td><td></td><td>LO</td><td>MO</td>
<td>ta</td><td>E</td><td>ta</td><td></td><td>ta</td><td></td><td>ta</td><td></td><td>ta</td><td></td><td>ta</td><td></td><td>ta</td><td></td><td>ta</td><td>ta</td>
<td>*-ta</td><td>'T*’</td><td></td><td></td><td>*—X</td><td>^*ta</td><td>**χ,</td><td>^*-χ.</td><td> ,*—»</td><td>,*ta.</td><td></td><td>**ta</td><td>y*ta</td><td>**ta</td><td>*-ta</td><td>**ta</td>
<td>X</td><td> 0</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td>
<td>X</td><td>CM</td><td>X</td><td>CO</td><td>X</td><td>co</td><td>X</td><td>co</td><td>CM</td><td>co</td><td>X</td><td>co</td><td>CM</td><td>X</td><td>X</td><td>rd</td>
<td>ta</td><td>κ</td><td>ta</td><td></td><td>ta</td><td>ta</td><td>ta</td><td>ta</td><td> «»</td><td></td><td>ta</td><td></td><td>ta</td><td>ta</td><td>ta</td><td>ta</td>
<td>-P</td><td>r-</td><td>-P</td><td> 6</td><td> 4-1</td><td></td><td> 4-»</td><td>s.</td><td> 4-></td><td> 3</td><td> 4-1</td><td> 3</td><td>-P</td><td>e.</td><td> 4-1</td><td> 3</td>
<td></td><td> 1</td><td></td><td></td><td> *</td><td></td><td>•ta*»</td><td></td><td>ta*»</td><td></td><td>ta*»</td><td></td><td> »—*</td><td></td><td>ta*»</td><td></td>
<td>o</td><td> 0</td><td>co</td><td>co</td><td>co</td><td>X</td><td>m</td><td>X</td><td>X</td><td>X</td><td>C0</td><td>X</td><td>CO</td><td>X</td><td>X</td><td>X</td>
<td>X</td><td> 00</td><td>rd</td><td>r-</td><td>rd</td><td>MO</td><td>rd</td><td>r-</td><td>ip</td><td>r-</td><td>rd</td><td>r—</td><td>rd</td><td>r-</td><td>Tp</td><td>MO</td>
<td>ta</td><td>ta</td><td>ta</td><td>ta</td><td>ta</td><td>ta</td><td>ta</td><td>ta</td><td>X</td><td>ta</td><td>ta</td><td>ta</td><td>ta</td><td>ta</td><td>X</td><td>ta</td>
<td></td><td>kO</td><td></td><td>kO</td><td></td><td>kO</td><td></td><td>kO</td><td>P'</td><td>kO</td><td></td><td>kO</td><td></td><td>MO</td><td>T</td><td>kO</td>
<td></td><td></td><td>CM 1</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>X 1</td><td></td>
<td></td><td></td><td>1 CO</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td> 1 05</td><td></td>
<td></td><td></td><td> 0)</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td> (0</td><td></td>
<td></td><td></td><td>rd</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td> <—1</td><td></td>
<td></td><td></td><td>•P</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>•P</td><td></td>
<td> 1</td><td></td><td>c</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>c</td><td></td>
<td> 1</td><td></td><td>Φ</td><td></td><td> 1</td><td></td><td> 1</td><td></td><td> 1</td><td></td><td> 1</td><td></td><td>t</td><td></td><td>Φ</td><td></td>
<td> •|</td><td></td><td>•P</td><td></td><td></td><td></td><td></td><td></td><td>ΐ</td><td></td><td></td><td></td><td>S</td><td></td><td>-P</td><td></td>
<td> 1</td><td></td><td>-P</td><td></td><td> 1</td><td></td><td> 1</td><td></td><td> 1</td><td></td><td> 1</td><td></td><td> 1</td><td></td><td> 4-1</td><td></td>
<td></td><td></td><td>rp</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>P</td><td></td>
<td></td><td></td><td>•P</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>O</td><td></td>
<td></td><td></td><td>-P</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td> <—1</td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>X</td><td></td>
<td></td><td></td><td> 1</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>U</td><td></td>
<td></td><td></td><td>LT)</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>1 X</td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>co I</td><td></td><td></td><td></td><td></td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>1 co</td><td></td><td></td><td></td><td></td><td></td>
<td><n</td><td></td><td>co</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>(d</td><td></td><td></td><td></td><td>X</td><td></td>
<td>(Ū</td><td></td><td> 1</td><td></td><td></td><td></td><td> 1</td><td></td><td></td><td></td><td>«“d</td><td></td><td></td><td></td><td> 1</td><td></td>
<td>r—1</td><td></td><td>co</td><td></td><td></td><td></td><td>co</td><td></td><td></td><td></td><td>•P</td><td></td><td></td><td></td><td> 05</td><td></td>
<td>•rd</td><td></td><td></td><td></td><td></td><td></td><td>(d</td><td></td><td></td><td></td><td>c</td><td></td><td></td><td></td><td>Ifl</td><td></td>
<td>C</td><td></td><td>rp</td><td></td><td></td><td></td><td>rp</td><td></td><td></td><td></td><td>c3</td><td></td><td></td><td></td><td>1—t</td><td></td>
<td> 0)</td><td></td><td>•P</td><td></td><td></td><td></td><td>•P</td><td></td><td></td><td></td><td>P</td><td></td><td></td><td></td><td>•P</td><td></td>
<td>Md</td><td></td><td>c</td><td></td><td></td><td></td><td>c</td><td></td><td></td><td></td><td>•P</td><td></td><td></td><td></td><td>c</td><td></td>
<td>r-d</td><td></td><td><d</td><td></td><td> |</td><td></td><td>rtj</td><td></td><td> 1</td><td></td><td>O4</td><td></td><td> 1</td><td></td><td> <3</td><td></td>
<td>•rd</td><td></td><td>P</td><td></td><td> •</td><td></td><td>P</td><td></td><td></td><td></td><td>O</td><td></td><td></td><td></td><td>P</td><td></td>
<td>-P</td><td></td><td>•P</td><td></td><td>Ί</td><td></td><td>•P</td><td></td><td>Ί</td><td></td><td>•P</td><td></td><td> *1</td><td></td><td>P</td><td></td>
<td>Φ</td><td></td><td>cx</td><td></td><td></td><td></td><td>cu</td><td></td><td></td><td></td><td>-P</td><td></td><td></td><td></td><td>cu</td><td></td>
<td></td><td></td><td> 0</td><td></td><td></td><td></td><td> 0</td><td></td><td></td><td></td><td> 0</td><td></td><td></td><td></td><td> 0</td><td></td>
<td>•H</td><td></td><td>P</td><td></td><td></td><td></td><td>P</td><td></td><td></td><td></td><td>P</td><td></td><td></td><td></td><td>P</td><td></td>
<td>P</td><td></td><td>Ό</td><td></td><td></td><td></td><td> 3</td><td></td><td></td><td></td><td>TJ</td><td></td><td></td><td></td><td> •3</td><td></td>
<td>-P |</td><td></td><td>•P</td><td></td><td></td><td></td><td>•P</td><td></td><td></td><td></td><td>•P</td><td></td><td></td><td></td><td>-P</td><td></td>
<td>1 kO</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td> <3</td><td></td><td></td><td></td><td>'S</td><td></td>
<td>ta</td><td></td><td>P</td><td></td><td></td><td></td><td>P</td><td></td><td></td><td></td><td>P</td><td></td><td></td><td></td><td>P</td><td></td>
<td></td><td></td><td>-P</td><td></td><td></td><td></td><td>P</td><td></td><td></td><td></td><td> 4-1</td><td></td><td></td><td></td><td> 4-1</td><td></td>
<td>ta</td><td></td><td>Φ</td><td></td><td></td><td></td><td>Φ</td><td></td><td></td><td></td><td>Φ</td><td></td><td></td><td></td><td>Φ</td><td></td>
<td>CM</td><td></td><td>-P</td><td></td><td></td><td></td><td> 4-1</td><td></td><td></td><td></td><td> 4-1</td><td></td><td></td><td></td><td> 4-1</td><td></td>
<td></td><td></td><td></td><td></td><td> 05</td><td></td><td></td><td></td><td> «</td><td></td><td></td><td></td><td>w</td><td></td><td></td><td></td>
<td></td><td></td><td></td><td></td><td>nj</td><td></td><td></td><td></td><td>Ifl</td><td></td><td></td><td></td><td><d</td><td></td><td></td><td></td>
<td>CO</td><td></td><td>m</td><td></td><td> <—1</td><td></td><td> 05</td><td></td><td>rp</td><td></td><td> 05</td><td></td><td>rp</td><td></td><td> 05</td><td></td>
<td>id</td><td></td><td> (0</td><td></td><td>•P</td><td></td><td>Ifl</td><td></td><td>•P</td><td></td><td>Ifl</td><td></td><td>•P</td><td></td><td>Φ</td><td></td>
<td>r—|</td><td></td><td>rd</td><td></td><td>CU</td><td></td><td>rd</td><td></td><td>a</td><td></td><td>1—I</td><td></td><td> 0,</td><td></td><td>rd</td><td></td>
<td>•rd</td><td></td><td>•P</td><td></td><td> 0</td><td></td><td>•P</td><td></td><td> 0</td><td></td><td>P</td><td></td><td>O</td><td></td><td>•P</td><td></td>
<td>-P</td><td></td><td>-P</td><td></td><td>P</td><td></td><td>4J</td><td></td><td>P</td><td></td><td> 4-1</td><td></td><td>P</td><td></td><td>-P</td><td></td>
<td>d)</td><td></td><td>ω</td><td></td><td>cu</td><td></td><td>Φ</td><td></td><td>cu</td><td></td><td>Φ</td><td></td><td>(X</td><td></td><td> <1></td><td></td>
<td>rd</td><td></td><td>CM</td><td></td><td>X</td><td></td><td>'T</td><td></td><td>X</td><td></td><td>MO</td><td></td><td>r-</td><td></td><td> 00</td><td></td>
<td>rd</td><td></td><td>rd</td><td></td><td> 1—1</td><td></td><td>rd</td><td></td><td>rd</td><td></td><td> »—1</td><td></td><td>rd</td><td></td><td>rd</td><td></td>
<td></td><td></td><td> •</td><td></td><td> •</td><td></td><td> •</td><td></td><td> •</td><td></td><td> •</td><td></td><td> •</td><td></td><td> •</td><td></td>
<td>CO</td><td></td><td>OO</td><td></td><td> 00</td><td></td><td> 00</td><td></td><td> 00</td><td></td><td></td><td></td><td> 00</td><td></td><td> 00</td><td></td>
U o
-P
<td colspan="2">X</td><td colspan="2">Χ-Χ</td><td colspan="2">X</td><td colspan="2">X</td><td colspan="2">X</td><td colspan="2">X</td><td colspan="4">X</td>
<td>z—</td><td></td><td>X</td><td></td><td>.z-fe</td><td></td><td>ΖΧ</td><td></td><td>z>.</td><td></td><td>z—fe,</td><td></td><td>fe,</td><td></td><td>Z-fe</td><td></td>
<td>X</td><td></td><td>»P</td><td></td><td>X</td><td></td><td>X</td><td></td><td>X</td><td></td><td>X</td><td></td><td>ZX</td><td></td><td>X</td><td></td>
<td>P</td><td></td><td>X</td><td></td><td>tP</td><td></td><td>P</td><td></td><td>P</td><td></td><td>rp</td><td></td><td>K</td><td></td><td>rH</td><td></td>
<td></td><td></td><td>X</td><td></td><td>X</td><td></td><td>X</td><td></td><td>X</td><td></td><td>X</td><td></td><td>P</td><td></td><td>X</td><td></td>
<td>S</td><td></td><td>Ό</td><td></td><td>T)</td><td></td><td>TJ</td><td></td><td>TJ</td><td></td><td>P</td><td></td><td>X</td><td></td><td>u</td><td></td>
<td></td><td></td><td>XM<*</td><td></td><td>X—iz</td><td></td><td>XX</td><td></td><td>X—*</td><td></td><td>fe—z</td><td></td><td>TJ</td><td></td><td>fe_x</td><td></td>
<td>LD</td><td></td><td>kO</td><td></td><td>kO</td><td></td><td>kO</td><td></td><td>LO</td><td></td><td> 0</td><td></td><td></td><td></td><td> 0</td><td></td>
<td>T</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>V*</td><td></td><td>in</td><td></td><td> 0</td><td></td><td> 10</td><td></td>
<td>X</td><td></td><td>X</td><td></td><td>X</td><td></td><td>X</td><td></td><td>X</td><td></td><td>X</td><td></td><td>LO</td><td></td><td>X</td><td></td>
<td>LO</td><td></td><td>LO</td><td></td><td>LO</td><td></td><td>kO</td><td></td><td>kO</td><td></td><td>kO</td><td></td><td>X</td><td></td><td>kO</td><td></td>
<td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>LO</td><td></td><td></td><td></td>
<td>X</td><td></td><td>X</td><td></td><td>X</td><td></td><td>X</td><td></td><td>X</td><td></td><td>X</td><td></td><td></td><td></td><td>X</td><td></td>
<td>ζ>></td><td></td><td>Z—fe</td><td></td><td></td><td></td><td>z--.</td><td></td><td>z></td><td></td><td>Z-fe</td><td></td><td>X</td><td></td><td>Z-fe</td><td></td>
<td>X</td><td>Χ-Χ</td><td>X</td><td>Z-fe.</td><td>X</td><td>Z-fe.</td><td>X</td><td></td><td>Ή</td><td>Z—fe</td><td>X</td><td></td><td>Z-fe</td><td></td><td>3ί</td><td></td>
<td>X</td><td>X</td><td>P</td><td>X</td><td>P</td><td>X</td><td>P</td><td>X</td><td>P</td><td>X</td><td>P</td><td></td><td>X</td><td></td><td>P</td><td></td>
<td> <.</td><td>P</td><td>X</td><td>tp</td><td>X</td><td>P</td><td>X</td><td><P</td><td>X</td><td>tP</td><td>fe.</td><td></td><td>P</td><td></td><td>X</td><td></td>
<td>X</td><td>X</td><td>X</td><td>X</td><td>-P</td><td>X</td><td>-P</td><td>fe.</td><td>P</td><td>X</td><td> 4-»</td><td></td><td>X</td><td></td><td>-P</td><td></td>
<td></td><td>TJ</td><td>TJ</td><td>T)</td><td>τί</td><td>TJ</td><td>TJ</td><td>TJ</td><td>TJ</td><td>T3</td><td>TJ</td><td></td><td>X</td><td></td><td>Ό</td><td></td>
<td></td><td>X—*</td><td>X—Z</td><td>«Χ-Χ</td><td>•χ**</td><td> *—</td><td>X—”</td><td>x—'</td><td>x—'</td><td>X—*</td><td>X-*·</td><td></td><td>X—r</td><td></td><td>XzZ</td><td></td>
<td>ro</td><td>m</td><td>ro</td><td>LO</td><td>ro</td><td>uo</td><td>co</td><td>LO</td><td>CO</td><td>m</td><td>r*</td><td></td><td>(X</td><td></td><td>r*</td><td></td>
<td>σι</td><td>r-</td><td>σι</td><td>r-</td><td>στ</td><td>t—-</td><td>στ</td><td>r-</td><td>στ</td><td>r-</td><td>O</td><td>Z-fe,</td><td> 0</td><td>Z—»</td><td> 0</td><td>Z-fe</td>
<td>X</td><td>X</td><td></td><td>X</td><td>X</td><td>κ</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td>
<td>IT)</td><td>kO</td><td>m</td><td>LO</td><td>LO</td><td>LO</td><td>LO</td><td>LO</td><td>LO</td><td>LO</td><td>LO</td><td>co</td><td>kO</td><td>ro</td><td>kO</td><td>ro</td>
<td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>X</td><td></td><td>X</td><td></td><td>X</td>
<td>X</td><td>X</td><td></td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>ε</td><td>X</td><td>ε</td><td>X</td><td>ε</td>
<td>Zfe</td><td>z^w</td><td>^«X</td><td></td><td> /«></td><td>Z—fe</td><td>Z-ki.</td><td>Z-fe</td><td>zx</td><td>zx</td><td>z—fe</td><td>χ-*’</td><td>z></td><td>χ-*</td><td>ZS</td><td>X—*</td>
<td>X</td><td>X</td><td>X</td><td>X</td><td>K</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>CM</td><td>X</td><td>CM</td><td>X</td><td>CM</td>
<td>CM</td><td>P</td><td>CM</td><td>«Ρ</td><td>CM</td><td>rP</td><td>CM</td><td>rp</td><td>CM</td><td>»P</td><td>CM</td><td>CO</td><td>CM</td><td>ro</td><td>CM</td><td>CO</td>
<td>X</td><td>X</td><td>X</td><td>X</td><td>χ</td><td>X</td><td>X</td><td>χ</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td></td>
<td>X</td><td>S</td><td>X</td><td> 3</td><td>P</td><td>T)</td><td>X</td><td>TJ</td><td>X</td><td>TJ</td><td>X</td><td>r-</td><td>X</td><td>r-</td><td> 4-1</td><td>r-</td>
<td></td><td></td><td>XfeZ</td><td></td><td>X—»</td><td></td><td>X-z</td><td>X—*</td><td>Xw*</td><td>xz</td><td>x*</td><td> 1</td><td>X—*</td><td> 1</td><td>X-*·</td><td> 1</td>
<td>m</td><td>ro</td><td>m</td><td>ro</td><td>LO</td><td>ro</td><td>LO</td><td>co</td><td>LO</td><td>n</td><td>LO</td><td> 0</td><td>LO</td><td> 0</td><td> 0</td><td>ro</td>
<td>P</td><td>LO</td><td>P</td><td>LO</td><td>«Ρ</td><td>kO</td><td>P</td><td>kO</td><td>P</td><td>LO</td><td>P</td><td> 0</td><td>rp</td><td> 0</td><td>CM</td><td> 0</td>
<td>X</td><td>χ</td><td>X</td><td>χ</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>v</td><td>X</td><td>X</td><td></td><td></td>
<td></td><td>kO</td><td></td><td>kO</td><td></td><td>kO</td><td></td><td>kO</td><td>«r</td><td>LO</td><td>rr</td><td>r-</td><td>’T</td><td>r-</td><td></td><td>r-</td>
CM
I to (fl
<img file="LT3295B_D0023.tif" />
C
Φ •H
X
G
O r—I
X υ
i m
n i
w <a
X •H et to /1 c
X to (D·
X to •d)
1—1 0) X c Φ *—l ao e£ ro to
<td>ro l</td><td colspan="2">V 1</td><td colspan="2">rt rp</td><td colspan="2">CO 1</td><td>ν’ 1</td>
<td>n</td><td>to</td><td></td><td>•P</td><td></td><td>to</td><td></td><td>to</td>
<td> (0</td><td>(fl</td><td></td><td>G</td><td></td><td>(fl</td><td></td><td> (0</td>
<td> 1—(</td><td>G</td><td></td><td>(fl</td><td></td><td>P</td><td></td><td>G</td>
<td>-G</td><td>•G</td><td></td><td>G</td><td></td><td>•P</td><td></td><td>•G</td>
<td>G</td><td>G</td><td></td><td>-G</td><td></td><td>c</td><td></td><td>G</td>
<td>(fl</td><td> (0</td><td> 1</td><td>Ch</td><td> 1</td><td> (3</td><td> 1</td><td>S</td>
<td>G •G</td><td>G -G</td><td>Ί</td><td>0 G</td><td>Ί</td><td>G •P</td><td>Ϊ</td><td>G G</td>
<td>Ch</td><td>Ch</td><td></td><td>4-J</td><td></td><td>Ch</td><td></td><td>Ch</td>
<td> 0</td><td>0 G</td><td></td><td>0 G</td><td></td><td>0 G</td><td></td><td>O Ū</td>
<td>TJ -G X</td><td>TJ •P X</td><td></td><td>τί •P X</td><td></td><td>Ό •P X</td><td></td><td>TJ -P X</td>
<td><3 G</td><td>13 G</td><td></td><td><3 G</td><td></td><td><3 G</td><td></td><td><3 G</td>
<td>X</td><td>X</td><td></td><td> 4-1</td><td></td><td> 44</td><td></td><td> 44</td>
<td>Φ</td><td>Φ</td><td></td><td>Φ</td><td></td><td>Φ</td><td></td><td>Φ</td>
<td>4J</td><td>4J</td><td></td><td> 44</td><td></td><td> 44</td><td></td><td> 44</td>
<td colspan="2">to</td><td colspan="2">to</td><td colspan="2">to</td><td colspan="2">to</td>
<td>(fl</td><td></td><td>(fl</td><td></td><td>(fl</td><td></td><td>(fl</td><td></td>
<td> 1—1</td><td>co</td><td> 1—1</td><td>to</td><td>G</td><td>to</td><td>G</td><td> (0</td>
<td>•G</td><td><d</td><td>•G</td><td>(fl</td><td>•G</td><td> (0</td><td>-G</td><td><d</td>
<td>Ch</td><td>•P</td><td>Ch</td><td>1—t</td><td>Ch</td><td>P</td><td>S*</td><td>rp</td>
<td>O</td><td>•P</td><td>O</td><td>•G</td><td> 0</td><td>•P</td><td> 0</td><td>•P</td>
<td>G</td><td> 44</td><td>G</td><td> 44</td><td>G</td><td>X</td><td>G</td><td>X</td>
<td>Ch</td><td>Φ</td><td>Ch</td><td>Φ</td><td>Ch</td><td>Φ</td><td>Ch</td><td>Φ</td>
<td>σι</td><td> 0</td><td>P</td><td>CM</td><td>ro</td><td>v</td><td>X</td><td>LD</td>
<td>P</td><td>CM</td><td>CM</td><td>CM</td><td>CM</td><td>CM</td><td>CM</td><td>CM</td>
<td> •</td><td> •</td><td> •</td><td> •</td><td> •</td><td></td><td> •</td><td> •</td>
<td>co</td><td> 00</td><td> 00</td><td> 00</td><td> 00</td><td> 00</td><td> 00</td><td> 00</td>
Nr. R<sub>x</sub> R<sub>2</sub> W fizikiniai duomenys: BMR: m. d. lyd.
<td>K</td><td colspan="2"> ·*</td><td colspan="3">k</td><td colspan="2">•k</td><td colspan="2">K</td><td colspan="2">«k</td><td colspan="2">h.</td><td></td>
<td></td><td></td><td>«—k.</td><td></td><td></td><td></td><td>««-k.</td><td></td><td>k</td><td></td><td>^-k</td><td></td><td>—«k</td><td></td><td>^—k,</td>
<td>E</td><td></td><td>E</td><td></td><td>E</td><td></td><td>E</td><td></td><td>E</td><td></td><td>E</td><td></td><td>E</td><td></td><td>E</td>
<td>rH</td><td></td><td>rH</td><td></td><td>rH</td><td></td><td>rH</td><td></td><td>rH</td><td></td><td>rH</td><td></td><td>rH</td><td></td><td>rH</td>
<td>K</td><td></td><td>K</td><td></td><td>K</td><td></td><td></td><td></td><td></td><td></td><td>K</td><td></td><td>«h</td><td></td><td></td>
<td>P</td><td></td><td>P</td><td></td><td>P</td><td></td><td>P</td><td></td><td>P</td><td></td><td>P</td><td></td><td>P</td><td></td><td>S</td>
<td></td><td></td><td>'k—*’</td><td></td><td>k—'</td><td></td><td>k»—*</td><td></td><td>k—-</td><td></td><td>k—*</td><td></td><td></td><td></td><td></td>
<td>o</td><td></td><td>o</td><td></td><td>o</td><td></td><td>CH</td><td></td><td>CH</td><td></td><td>CH</td><td></td><td>CH</td><td></td><td>CO</td>
<td>m</td><td></td><td>LO</td><td></td><td>LO</td><td></td><td>LO</td><td></td><td>LO</td><td></td><td>LO</td><td></td><td>LO</td><td></td><td>LO</td>
<td>K</td><td></td><td>k»</td><td></td><td>h.</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td>h.</td>
<td>LO</td><td></td><td>LO</td><td></td><td>kO</td><td></td><td>kO</td><td></td><td>LO</td><td></td><td>kO</td><td></td><td>kO</td><td></td><td>LO</td>
<td>k</td><td></td><td>h.</td><td></td><td> *</td><td></td><td>hl</td><td></td><td>kl</td><td></td><td>hi</td><td></td><td>kk</td><td></td><td></td>
<td>«kk</td><td></td><td>«—kk</td><td></td><td>—kk</td><td></td><td>-—k</td><td></td><td>^«k</td><td></td><td>,^-k,</td><td></td><td>«kk</td><td></td><td>k»</td>
<td>E</td><td></td><td>E</td><td></td><td>K</td><td></td><td>oc</td><td></td><td>E</td><td></td><td>K</td><td></td><td>oc</td><td></td><td>E</td>
<td>rH</td><td></td><td>rH</td><td></td><td>rH</td><td></td><td>rH</td><td></td><td>rH</td><td></td><td>rH</td><td></td><td>rH</td><td></td><td>rH</td>
<td>h,</td><td></td><td>h.</td><td></td><td></td><td></td><td></td><td></td><td>K</td><td></td><td></td><td></td><td>,k</td><td></td><td></td>
<td>P</td><td></td><td>P</td><td></td><td>•U</td><td></td><td>-U</td><td></td><td>P</td><td></td><td> 4-></td><td></td><td> 4-1</td><td></td><td>P</td>
<td>P</td><td></td><td>P</td><td></td><td>Ό</td><td></td><td>τί</td><td></td><td>P</td><td></td><td>Ό</td><td></td><td>Ό</td><td></td><td>P</td>
<td></td><td></td><td></td><td></td><td>**—r</td><td></td><td></td><td></td><td>k——</td><td></td><td>•k—*</td><td></td><td>k—·</td><td></td><td>*k—'</td>
<td>r-</td><td></td><td>r*</td><td></td><td>r-</td><td></td><td>o</td><td></td><td>O</td><td></td><td>CO</td><td></td><td>CO</td><td></td><td>CN</td>
<td>o</td><td>«k</td><td>o</td><td></td><td>o</td><td></td><td>rH</td><td></td><td>rH</td><td></td><td>rH</td><td></td><td>rH</td><td></td><td>rH</td>
<td>«k</td><td>XJ</td><td></td><td>E</td><td>h,</td><td>K</td><td>k.</td><td></td><td>»k</td><td></td><td>k»</td><td></td><td>hb</td><td></td><td></td>
<td>kO</td><td>co</td><td>kO</td><td>co</td><td>kO</td><td>co</td><td>kO</td><td></td><td>kO</td><td></td><td>kO</td><td></td><td>kO</td><td></td><td>kO</td>
<td></td><td>k.</td><td></td><td>k.</td><td></td><td>kl</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td>
<td>h.</td><td>ε</td><td>v</td><td>ε</td><td>K</td><td>ε</td><td>h.</td><td></td><td>K</td><td></td><td>h.</td><td></td><td>hk</td><td></td><td>h.</td>
<td>««—«k</td><td></td><td>——k</td><td></td><td></td><td><«—Χ</td><td>—-k.</td><td>—•«k</td><td>——k</td><td>k»</td><td>z-k</td><td>——k</td><td>—-ki</td><td>z~k</td><td>z—k.</td>
<td>K</td><td>CH</td><td>K</td><td>kO</td><td>E</td><td>kO</td><td>E</td><td>E</td><td></td><td>E</td><td>E</td><td>E</td><td>E</td><td>E</td><td>E</td>
<td>CN</td><td>CO</td><td>CN</td><td>no</td><td>CH</td><td>co</td><td>CH</td><td>CH</td><td>CN</td><td>CH</td><td>CH</td><td>CH</td><td>CH</td><td>CH</td><td>CH</td>
<td>•k</td><td></td><td></td><td>K</td><td>hl</td><td>h,</td><td>k.</td><td> *,</td><td>k.</td><td>k.</td><td>k.</td><td>kk</td><td>hi</td><td>hi</td><td>hi</td>
<td> 4-»</td><td>r-</td><td>P</td><td>r·*</td><td>P</td><td>r-</td><td>P</td><td>to</td><td>P</td><td>G</td><td>P</td><td>G</td><td>P</td><td>G</td><td>P</td>
<td> ·*—-</td><td> 1</td><td></td><td> 1</td><td>kk—'</td><td> 1</td><td>k—</td><td>•k—r</td><td>k—</td><td>k—*</td><td> —-</td><td> —-</td><td> ·*—*</td><td> ·*—'</td><td>k—</td>
<td>O</td><td>co</td><td>r-</td><td>o</td><td>r*·</td><td>o</td><td>o</td><td>LO</td><td>o</td><td>LO</td><td>o</td><td>γ-</td><td>O</td><td>r-*</td><td>o</td>
<td>CN</td><td>o</td><td>rH</td><td>o</td><td>rH</td><td>o</td><td>CN</td><td>o</td><td>CN</td><td>O</td><td>CH</td><td>ο</td><td>CN</td><td>o</td><td>CN</td>
<td></td><td> *.</td><td> •</td><td>kk</td><td>v</td><td>v</td><td>kl</td><td></td><td>ki</td><td>h.</td><td>κ</td><td>k</td><td>ki</td><td></td><td>hk</td>
<td></td><td>r*-</td><td></td><td>r-</td><td></td><td></td><td></td><td></td><td></td><td>r-</td><td></td><td>r-</td><td></td><td>r*</td><td></td>
<td colspan="8">co 1</td>
<td></td><td></td><td></td><td>t G</td><td></td><td></td><td></td><td></td>
<td></td><td></td><td></td><td>G</td><td></td><td></td><td></td><td></td>
<td></td><td></td><td></td><td> —1</td><td></td><td></td><td></td><td></td>
<td></td><td></td><td></td><td>G</td><td></td><td></td><td></td><td></td>
<td></td><td></td><td></td><td>G</td><td></td><td></td><td></td><td></td>
<td> 1</td><td> 1</td><td>co</td><td>Φ</td><td> 1</td><td> 1</td><td> 1</td><td> 1</td>
<td></td><td> ™|</td><td> 1</td><td>•G</td><td>s</td><td>i</td><td>s</td><td></td>
<td>i</td><td> 1</td><td>G</td><td>P</td><td> 1</td><td>t</td><td> 1</td><td> 1</td>
<td></td><td></td><td>G</td><td>G</td><td></td><td></td><td></td><td></td>
<td></td><td></td><td> <—1</td><td>O</td><td></td><td></td><td></td><td></td>
<td></td><td></td><td>•H</td><td> —1</td><td></td><td></td><td></td><td></td>
<td></td><td></td><td>G</td><td>E</td><td></td><td></td><td></td><td></td>
<td></td><td></td><td>Φ</td><td>U</td><td></td><td></td><td></td><td></td>
<td></td><td></td><td>-H</td><td> 1</td><td></td><td></td><td></td><td></td>
<td></td><td></td><td>P</td><td>CH</td><td></td><td></td><td></td><td></td>
<td></td><td>co I</td><td colspan="5">CO</td><td>co I</td>
<td></td><td>G</td><td>1 G</td><td></td><td></td><td></td><td></td><td>1 G</td>
<td></td><td>G</td><td>G</td><td>co</td><td></td><td>•T</td><td></td><td>G</td>
<td></td><td>r—1</td><td>Ή</td><td> 1</td><td></td><td> 1</td><td></td><td>r—t</td>
<td></td><td>•G</td><td>•G</td><td>G</td><td></td><td>G</td><td></td><td>G</td>
<td></td><td>G</td><td>C</td><td>G</td><td></td><td>G</td><td></td><td>C</td>
<td></td><td>G</td><td>G</td><td> —1</td><td></td><td> —1</td><td></td><td>G</td>
<td></td><td>G</td><td>G</td><td>G</td><td></td><td>•G</td><td></td><td>G</td>
<td></td><td>•G</td><td>•G</td><td>G</td><td></td><td>G</td><td></td><td>-G</td>
<td> 1</td><td>et</td><td>et</td><td>G</td><td> 1</td><td>G</td><td> 1</td><td>et</td>
<td> •</td><td>o</td><td> 0</td><td>G</td><td></td><td>G</td><td></td><td> 0</td>
<td>Ί</td><td>•G</td><td>•G</td><td>G</td><td>Ϊ</td><td>-G</td><td>j</td><td>•G</td>
<td></td><td>P</td><td>P</td><td>et</td><td></td><td>et</td><td></td><td>P</td>
<td></td><td>O</td><td> 0</td><td>o</td><td></td><td>o</td><td></td><td>O</td>
<td></td><td>G</td><td>G</td><td>G</td><td></td><td>G</td><td></td><td>G</td>
<td></td><td>P</td><td>P</td><td>P</td><td></td><td>P</td><td></td><td>P</td>
<td></td><td>•H</td><td>•Ή</td><td>•r4</td><td></td><td>•G</td><td></td><td>•rH</td>
<td></td><td>E</td><td>E</td><td>E</td><td></td><td>E</td><td></td><td>E</td>
<td></td><td>G</td><td>fO</td><td>G</td><td></td><td>G</td><td></td><td>G</td>
<td></td><td>G</td><td>G</td><td>G</td><td></td><td>G</td><td></td><td>G</td>
<td></td><td>P</td><td>P</td><td>P</td><td></td><td>P</td><td></td><td>P</td>
<td></td><td>Φ</td><td>Φ</td><td>Φ</td><td></td><td>Φ</td><td></td><td>Φ</td>
<td></td><td>P</td><td>P</td><td>P</td><td></td><td>P</td><td></td><td>P</td>
<td>G</td><td></td><td>G</td><td></td><td>G</td><td></td><td>G</td><td></td>
<td>G</td><td></td><td>G</td><td></td><td>G</td><td></td><td>G</td><td></td>
<td> —1</td><td>G</td><td> »—1</td><td>G</td><td> —1</td><td>G</td><td>i—1</td><td>co</td>
<td>•G</td><td>G</td><td>-G</td><td>G</td><td>•G</td><td>G</td><td>•G</td><td> (0</td>
<td>et</td><td>r—1</td><td>et</td><td>rH</td><td>et</td><td> <—1</td><td>et</td><td> <—1</td>
<td> 0</td><td>•G</td><td> 0</td><td>-G</td><td> 0</td><td>G</td><td>o</td><td>•H</td>
<td>G</td><td>P</td><td>G</td><td>P</td><td>G</td><td>P</td><td>G</td><td> 4-)</td>
<td>et</td><td>Φ</td><td>et</td><td>Φ</td><td>et</td><td>Φ</td><td>et</td><td>Φ</td>
<td>Γ-</td><td> 00</td><td>σ</td><td>O</td><td>rH</td><td>CH</td><td>co</td><td></td>
<td>ΓΗ</td><td>CH</td><td>CH</td><td>co</td><td>C0</td><td>CO</td><td>co</td><td>co</td>
<td> 00</td><td> 00</td><td>co</td><td> 00</td><td> 00</td><td> 00</td><td> 00</td><td> 00</td>
Ū ė
<td colspan="2">k</td><td colspan="4">k</td><td colspan="2">k</td><td colspan="2"></td><td colspan="2">k</td>
<td></td><td></td><td>XX</td><td></td><td></td><td></td><td>XX</td><td></td><td>χχ</td><td></td><td>XX</td><td></td>
<td>E</td><td></td><td>E</td><td></td><td></td><td></td><td>E</td><td></td><td>E</td><td></td><td>E</td><td></td>
<td>rH</td><td></td><td>rH</td><td></td><td></td><td>XX</td><td>rH</td><td></td><td>rH</td><td></td><td>rH</td><td></td>
<td>k</td><td></td><td>X</td><td></td><td></td><td>E</td><td>X</td><td></td><td>k</td><td></td><td>k</td><td></td>
<td>S</td><td></td><td>Ό</td><td></td><td></td><td>rH</td><td>T3</td><td></td><td>Ό</td><td></td><td>Ό</td><td></td>
<td></td><td></td><td>kX</td><td></td><td></td><td>k</td><td>kX</td><td></td><td>kX</td><td></td><td>kX</td><td></td>
<td>E</td><td></td><td>cn</td><td></td><td></td><td>CO</td><td>E</td><td></td><td>E</td><td></td><td>E</td><td></td>
<td>E</td><td></td><td>CO</td><td></td><td></td><td>k-r</td><td>E</td><td></td><td>E</td><td></td><td>E</td><td></td>
<td>k</td><td></td><td>k</td><td></td><td></td><td>co</td><td>k</td><td></td><td>k</td><td></td><td>k</td><td></td>
<td>LO</td><td></td><td>LO</td><td></td><td></td><td>o</td><td>E</td><td></td><td>E</td><td></td><td>E</td><td></td>
<td>k</td><td></td><td>k</td><td></td><td>k</td><td>r-</td><td>k</td><td></td><td>k</td><td></td><td>k</td><td></td>
<td></td><td></td><td>χχ</td><td></td><td>XX</td><td></td><td>,χ</td><td></td><td>χχ</td><td></td><td>XX</td><td></td>
<td>E</td><td></td><td>E</td><td>xx</td><td>E</td><td>k</td><td>E</td><td>χχ</td><td>E</td><td>χχ</td><td>E</td><td>XX</td>
<td>rH</td><td></td><td>rH</td><td>X!</td><td>rH</td><td>X</td><td>rH</td><td>E</td><td>rH</td><td>Ή</td><td>rH</td><td>E</td>
<td>k</td><td></td><td>k</td><td>rH</td><td>X</td><td>E</td><td>k</td><td>rH</td><td>k</td><td>rH</td><td>k</td><td>τ-H</td>
<td>dJ</td><td></td><td>G</td><td>k</td><td>G</td><td>rH</td><td>G</td><td>k</td><td>G</td><td>k</td><td>G</td><td>k</td>
<td>Ό</td><td></td><td>Ό</td><td>co</td><td>Ό</td><td>k</td><td>Ό</td><td>CO</td><td>Ό</td><td>CO</td><td>Ό</td><td>to</td>
<td>•fccr</td><td></td><td> »—*·</td><td>kX</td><td>k—*</td><td>CO</td><td>k—*</td><td>k—r</td><td>k—<*</td><td>kx</td><td>k-*</td><td>kx</td>
<td>CM</td><td></td><td>o</td><td>CO</td><td>O</td><td></td><td>O</td><td>CO</td><td>O</td><td>co</td><td>O</td><td>co</td>
<td>rH</td><td></td><td>o</td><td>o</td><td>o</td><td>co</td><td>o</td><td>o</td><td>o</td><td>o</td><td>o</td><td>o</td>
<td>k</td><td></td><td>k</td><td>k</td><td>k</td><td> 00</td><td>k</td><td>k</td><td>x</td><td>k</td><td>k</td><td>k</td>
<td>LD</td><td></td><td>LD</td><td>r-</td><td>LD</td><td>k</td><td>LD</td><td>r-</td><td>LD</td><td>r~</td><td>LD</td><td>r-</td>
<td></td><td></td><td></td><td></td><td></td><td>LD</td><td></td><td></td><td></td><td></td><td></td><td></td>
<td>k</td><td></td><td>k</td><td>k</td><td>k</td><td>k</td><td>k</td><td>k</td><td>k</td><td>k</td><td>k</td><td>k</td>
<td>XX</td><td>X</td><td>XX</td><td>χχ</td><td></td><td>XX</td><td>XX</td><td>XX</td><td>X</td><td>XX</td><td>XX</td><td>XX</td>
<td>E</td><td>E</td><td>E</td><td>E</td><td>E</td><td>E</td><td>E</td><td>E</td><td>E</td><td>E</td><td>E</td><td>E</td>
<td>E</td><td>CM</td><td>E</td><td>rH</td><td>CM</td><td>rH</td><td>CM</td><td>rH</td><td>CM</td><td>rH</td><td>CM</td><td>rH</td>
<td>X</td><td>k</td><td>k</td><td>k</td><td>k</td><td>k</td><td>k</td><td>k</td><td>k</td><td>k</td><td>k</td><td>k</td>
<td>G</td><td>CO</td><td>G</td><td>to</td><td>G</td><td>Ό</td><td>G</td><td>CO</td><td>G</td><td>CO</td><td>G</td><td>to</td>
<td>X»/</td><td>X—'</td><td>k-*·</td><td>k**</td><td>k»</td><td>k-r</td><td>XX</td><td>•k*»</td><td>k*·</td><td>kX</td><td>kx</td><td>kx</td>
<td>O</td><td>o</td><td>r-</td><td>CO</td><td>r·</td><td>CO</td><td>r*</td><td>CO</td><td>r~</td><td>CO</td><td>o</td><td>co</td>
<td>CM</td><td>rH</td><td>rH</td><td> 00</td><td>rH</td><td>co</td><td>rH</td><td> 00</td><td>rH</td><td> 00</td><td>CM</td><td> 00</td>
<td>k</td><td>k</td><td>k</td><td>k</td><td>k</td><td>k</td><td>k</td><td>X</td><td>k</td><td>k</td><td>k</td><td>k</td>
<td>N*</td><td></td><td></td><td>E</td><td>Ν’</td><td>E</td><td>N·</td><td>LD</td><td>Ν’</td><td>LD</td><td>Ν’</td><td>E</td>
<td colspan="3">E 1</td><td>E</td>
<td>to</td><td></td><td></td><td> 1</td>
<td> (0</td><td></td><td></td><td>to</td>
<td>G</td><td></td><td></td><td>fl</td>
<td>•H</td><td></td><td></td><td>i—t</td>
<td>C</td><td></td><td></td><td>-G</td>
<td>Φ</td><td> 1</td><td> 1</td><td>C</td>
<td>-G</td><td>S</td><td> 5</td><td>Φ</td>
<td>G</td><td> 1</td><td> 1</td><td>•G</td>
<td>G</td><td></td><td></td><td>G</td>
<td>O</td><td></td><td></td><td>G</td>
<td>G</td><td></td><td></td><td> 0</td>
<td>E</td><td></td><td></td><td>E</td>
<td>U |</td><td></td><td></td><td>U 1</td>
<td>E</td><td></td><td></td><td>UO</td>
E
I m
<td colspan="2">C0 1</td><td>’T 1</td><td>Ν’ 1</td><td>id rH</td>
<td>to fl rH</td><td></td><td>to <d rH</td><td>to fl i—1</td><td>•rd §</td>
<td>•rd S</td><td> 1</td><td>rd i</td><td>•G S</td><td>G •rd ct</td>
<td>G</td><td></td><td>G</td><td>G</td><td>o</td>
<td>•rd</td><td>Ί</td><td>•H</td><td>rd</td><td>•rd</td>
<td>Ct</td><td></td><td>Ct</td><td>Ct</td><td>G</td>
o o o o ·$ -S E E •rd *rd Ή -rd χ; x: x!
nj <d id rd to
G •H m
Φ·
G
M •Φ i—I Φ G C Φ
<td></td><td>G</td><td></td><td>G</td><td>G</td><td>G</td>
<td></td><td>Φ</td><td></td><td>Φ</td><td>Φ</td><td>Φ</td>
<td></td><td>G</td><td></td><td>G</td><td>G</td><td>G</td>
<td>to</td><td></td><td>CO</td><td></td><td>to</td><td></td>
<td>fl</td><td></td><td>fd</td><td></td><td>fl</td><td></td>
<td>rH</td><td>to</td><td>r-1</td><td>to</td><td>r-H</td><td> ' 10</td>
<td>•rd</td><td>fl</td><td>♦rd</td><td>fl</td><td>•rd</td><td>fl</td>
<td>Ct</td><td> »—1</td><td>Ct</td><td> '—1</td><td>Ct</td><td>i—1</td>
<td>o</td><td>-G</td><td>o</td><td>•G</td><td> 0</td><td>-G</td>
<td>G</td><td>G</td><td>G</td><td>G</td><td>G</td><td>G</td>
<td>Ct</td><td>Φ</td><td>Ct</td><td>Φ</td><td>Ct</td><td>Φ</td>
<td>E</td><td>E</td><td>r~</td><td>CO</td><td>σ</td><td>O</td>
<td>E</td><td>E</td><td>E</td><td>E</td><td>E</td><td>Ν’</td>
<td>CO</td><td> 00</td><td>CO</td><td>E</td><td>co</td><td>E</td>
.41 propilas - 4,20(t,2H), 6,00(dt, 1H), 6,33 (d, 1H)
6, 83(s,lH), 7,03(s,lH) oo
M-HO - HJ<sup>Z</sup>HJ<sup>Z</sup>H3-OH
<img file="LT3295B_D0024.tif" />
lentelė
<img file="LT3295B_D0025.tif" />
10.09 etilas tetrahidropiranilas-4 - 91-93
T) ė
ra
Ή
N
Ή
MH fe
<td colspan="2">fe</td><td colspan="2">fe.</td><td>fe</td><td colspan="3">fe</td><td colspan="2">fe</td><td colspan="2">fe</td><td colspan="2">fe</td><td colspan="2">fe</td>
<td>—fe.</td><td></td><td>fe.</td><td></td><td>z—fe.</td><td></td><td>z—fe</td><td></td><td>Z—fe</td><td></td><td>Z-fe.</td><td></td><td>zZ—X</td><td></td><td>zz^fe</td><td></td>
<td>a</td><td></td><td>a</td><td></td><td>te</td><td></td><td>a</td><td></td><td>a</td><td></td><td>a</td><td></td><td>a</td><td></td><td>a</td><td></td>
<td>rH</td><td></td><td>rH</td><td></td><td>CM</td><td></td><td>rH</td><td></td><td>rH</td><td></td><td>rH</td><td></td><td>rH</td><td></td><td>rH</td><td></td>
<td>v</td><td></td><td>fe.</td><td></td><td>fe</td><td></td><td></td><td></td><td></td><td></td><td>fe</td><td></td><td>fe</td><td></td><td>fe</td><td></td>
<td>ε</td><td></td><td>ε</td><td></td><td>a</td><td>a</td><td>ε.</td><td></td><td>ε.</td><td></td><td>ε.</td><td></td><td>ε.</td><td></td><td>ε.</td><td></td>
<td></td><td></td><td>fe—'</td><td></td><td>fe—*</td><td>rH</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td>
<td>o</td><td></td><td>o</td><td></td><td>CN</td><td></td><td>o</td><td></td><td>o</td><td></td><td>o</td><td></td><td>kO</td><td></td><td>kO</td><td></td>
<td></td><td></td><td>σ></td><td></td><td>r—1</td><td>ε.</td><td> <71</td><td></td><td>cn</td><td></td><td><n</td><td></td><td>o</td><td></td><td>o</td><td></td>
<td> <</td><td></td><td>fe</td><td></td><td>k</td><td></td><td>fe</td><td></td><td>fe</td><td></td><td>fe</td><td></td><td>fe</td><td></td><td>fe</td><td></td>
<td>kO</td><td></td><td>kO</td><td></td><td></td><td>co</td><td>lf)</td><td></td><td>lf)</td><td></td><td>lf)</td><td></td><td>kO</td><td></td><td>vo</td><td></td>
<td></td><td></td><td></td><td></td><td></td><td>LO fe</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td>
<td></td><td></td><td>fe.</td><td></td><td></td><td>kO</td><td>fe</td><td></td><td>fe</td><td></td><td>fe</td><td></td><td>fe</td><td></td><td>fe</td><td></td>
<td>Z—*fe</td><td></td><td></td><td></td><td></td><td></td><td>zz—fe</td><td></td><td>Z—.,</td><td></td><td>Z*—k</td><td></td><td>z—fe</td><td></td><td>z^fe.</td><td></td>
<td>a</td><td></td><td>te</td><td></td><td></td><td>fe</td><td>a</td><td></td><td>a</td><td>z^</td><td>a</td><td></td><td>a</td><td></td><td>a</td><td></td>
<td>rH</td><td></td><td>r—1</td><td></td><td></td><td>z—fe</td><td>CN</td><td>a</td><td>CN</td><td>te</td><td>CN</td><td>te</td><td>rH</td><td></td><td>rH</td><td></td>
<td>fe.</td><td></td><td>fe</td><td></td><td></td><td>a</td><td>fe</td><td>T<sup>-</sup>1</td><td>fe</td><td>rH</td><td>fe</td><td>rH</td><td>fe</td><td></td><td>fe</td><td></td>
<td>S</td><td></td><td> £</td><td></td><td></td><td>rH</td><td>a</td><td></td><td>a</td><td>fe</td><td>a</td><td>fe</td><td>ε.</td><td></td><td>£į</td><td></td>
<td></td><td></td><td>fe—'</td><td></td><td></td><td>fe</td><td>fe—·</td><td>ε</td><td>•fe—</td><td>ε</td><td>fe—</td><td>g</td><td></td><td></td><td></td><td></td>
<td>o</td><td></td><td>o</td><td></td><td></td><td> £</td><td>CN</td><td></td><td>CM</td><td></td><td>CN</td><td></td><td>o</td><td></td><td>o</td><td></td>
<td> 00</td><td></td><td> 00</td><td></td><td></td><td></td><td>rH</td><td>co</td><td>rH</td><td>Γ9</td><td>rH</td><td>en</td><td>σι</td><td></td><td>en</td><td></td>
<td>fe</td><td></td><td>fe</td><td></td><td></td><td>kO</td><td></td><td>lf)</td><td>fe</td><td>LO</td><td>fe</td><td>m</td><td>fe</td><td></td><td>fe</td><td></td>
<td>kO</td><td></td><td>kO</td><td></td><td></td><td>o</td><td></td><td>fe</td><td></td><td></td><td></td><td></td><td>LO</td><td></td><td>Lf)</td><td></td>
<td></td><td></td><td></td><td></td><td></td><td>fe</td><td></td><td>kO</td><td></td><td>kO</td><td></td><td>kO</td><td></td><td></td><td></td><td></td>
<td></td><td></td><td></td><td></td><td></td><td>kO</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td>
<td> <</td><td></td><td>fe</td><td></td><td>fe</td><td>fe</td><td>fe</td><td>fe</td><td>fe</td><td>fe</td><td></td><td></td><td>fe</td><td></td><td>fe</td><td></td>
<td></td><td></td><td>z—fe</td><td>z—fe</td><td>z—fe,</td><td>z^-fe</td><td>Z—fe.</td><td>zz-fe</td><td>z—></td><td>z—χ</td><td>z**fe.</td><td>Z.—</td><td>z—fe</td><td>Z—fe</td><td>Z—fe</td><td>z—»</td>
<td>a</td><td>a</td><td>X</td><td>a</td><td>a</td><td>X</td><td>a</td><td>a</td><td>a</td><td>X</td><td>a</td><td>te</td><td>a</td><td>a</td><td>te</td><td>a</td>
<td>CN</td><td>rH</td><td>CM</td><td>rH</td><td>CN</td><td>rH</td><td>CN</td><td>rH</td><td>CN</td><td>rH</td><td>CN</td><td>rH</td><td>CN</td><td>rH</td><td>CM</td><td>rH</td>
<td>fe</td><td>fe.</td><td>K.</td><td> ·«.</td><td>fe</td><td>fe</td><td>fe</td><td></td><td>fe</td><td>fe</td><td></td><td>κ</td><td>fe</td><td>fe</td><td></td><td>κ</td>
<td>a</td><td>ε</td><td>4J</td><td>ε</td><td>ε</td><td>ε</td><td>ε</td><td></td><td>ε.</td><td> 3</td><td> 3</td><td> 3</td><td>a</td><td>ε.</td><td> 4-></td><td>ε.</td>
<td>fe—o</td><td>fe—</td><td>fe—-</td><td>fe—·</td><td>fe—r</td><td>fe—’</td><td>fe—</td><td></td><td></td><td></td><td></td><td></td><td>fe—</td><td></td><td>fe—</td><td></td>
<td>r-</td><td>o</td><td>Γ</td><td>o</td><td>O</td><td>o</td><td>o</td><td>vo</td><td>o</td><td>kO</td><td>o</td><td>kO</td><td>CN</td><td>co</td><td>CN</td><td>co</td>
<td>o</td><td>rH</td><td>O</td><td>rH</td><td>ΟΊ</td><td>O)</td><td>CPi</td><td>o</td><td>o</td><td>o</td><td>o</td><td>o</td><td>rH</td><td>lf)</td><td>rH</td><td>lf)</td>
<td></td><td>fe.</td><td>fe</td><td>fe</td><td>i*.</td><td></td><td>fe</td><td>fe</td><td>fe</td><td>fe</td><td>fe</td><td>fe</td><td></td><td>fe</td><td>fe</td><td>fe</td>
<td></td><td>r*·</td><td></td><td>r-</td><td>on</td><td>Lf)</td><td>m</td><td>kO</td><td></td><td>kO</td><td></td><td>kO</td><td></td><td>kO</td><td>M</td><td>vo</td>
CN
I ra ra o
P •H a
rH •rl
H-J i
I ra >1
C
P ra
Φ a
ra -Φ <—i ra a
G
Φ
<td>co I</td><td></td><td></td><td></td><td></td><td></td><td>co |</td>
<td>ra</td><td></td><td></td><td></td><td></td><td></td><td>1 m</td>
<td>ra</td><td></td><td>co</td><td></td><td>•fl</td><td></td><td>ra</td>
<td>i—t</td><td></td><td> 1</td><td></td><td> 1</td><td></td><td> .—1</td>
<td>•P</td><td></td><td>ra</td><td></td><td>ra</td><td></td><td>•P</td>
<td>G</td><td></td><td>ra</td><td></td><td>ra</td><td></td><td>c</td>
<td>ra</td><td></td><td>«-P</td><td></td><td>rp</td><td></td><td>ra</td>
<td>P</td><td></td><td>-P</td><td></td><td>•P</td><td></td><td>P</td>
<td>•P</td><td></td><td>G</td><td></td><td>c</td><td></td><td>•P</td>
<td>g</td><td> 1</td><td>ra</td><td> 1</td><td>ra</td><td> 1</td><td>G</td>
<td>o •P</td><td>T</td><td>P •P</td><td>i</td><td>P P</td><td>Ί</td><td>O •P</td>
<td>a</td><td></td><td>G</td><td></td><td>G</td><td></td><td>a</td>
<td>o</td><td></td><td> 0</td><td></td><td>o</td><td></td><td>o</td>
<td>K</td><td></td><td>P</td><td></td><td>P</td><td></td><td>P</td>
<td>ό</td><td></td><td>Ό</td><td></td><td> -3</td><td></td><td>T)</td>
<td>•r|</td><td></td><td>•rl</td><td></td><td>•rl</td><td></td><td>•H</td>
<td></td><td></td><td>a ra</td><td></td><td>a ra</td><td></td><td></td>
<td>P</td><td></td><td>P</td><td></td><td>P</td><td></td><td>P</td>
<td>a</td><td></td><td>a</td><td></td><td>a</td><td></td><td>a</td>
<td>ra</td><td></td><td>φ</td><td></td><td>Φ</td><td></td><td>φ</td>
<td>a</td><td></td><td>a</td><td></td><td>a</td><td></td><td>a</td>
<td colspan="2">ra</td><td></td><td colspan="3">ra</td><td colspan="2">ra</td><td></td>
<td>ra</td><td></td><td> <0</td><td></td><td>ra</td><td></td><td>ra</td><td></td><td>tfl</td>
<td>a</td><td></td><td>rH</td><td>ra</td><td> 1—1</td><td>w</td><td> >—1</td><td>m</td><td>rH</td>
<td>-P</td><td><T5</td><td>•rH</td><td>ra</td><td>•P</td><td></td><td>•P</td><td>ra</td><td>•r|</td>
<td>G</td><td>rH</td><td>Ch</td><td>rH</td><td>G</td><td>rH</td><td>G</td><td>rH</td><td>Λ</td>
<td>o</td><td>••H</td><td> 0</td><td>♦H</td><td> 0</td><td>•rl</td><td>O</td><td>•rH</td><td> 0</td>
<td>P</td><td>-U</td><td>M</td><td>a</td><td>P</td><td> 4~></td><td>P</td><td> 4-></td><td>n</td>
<td>G</td><td>Φ</td><td></td><td>φ</td><td>G</td><td>Φ</td><td>G</td><td>Φ</td><td>Λ</td>
<td>o</td><td>rH</td><td>CM</td><td>CO</td><td>a</td><td>Lf)</td><td>kO</td><td>r-</td><td> 00</td>
<td>’—t</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td><td>i—H</td><td> .—1</td><td>rH</td><td>rH</td>
<td>o</td><td>O</td><td>O</td><td>O</td><td>O</td><td>O</td><td>o</td><td>O</td><td>O</td>
<td> 1—1</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td><td>Ip</td><td>rH</td><td>rH</td>
<td>K</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td colspan="2">X</td>
<td>rH</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td><td></td><td>rH</td>
<td></td><td>fe</td><td>fe</td><td></td><td>fe</td><td>fe</td><td>fe</td><td>fe</td><td></td><td>fe</td>
<td>ε</td><td>ε</td><td>ε</td><td>ε</td><td>ε</td><td>ε</td><td>ε</td><td>ε</td><td></td><td>ε</td>
<td>fe—*</td><td>fe-*</td><td>fe—*</td><td>fe—'</td><td>fe-*</td><td>fe—*</td><td>fe—*</td><td>fe-*</td><td></td><td>fe—*</td>
<td>r-</td><td>Γ</td><td>r-</td><td>r*</td><td>r-</td><td>r*“</td><td>o</td><td>o</td><td></td><td> 0</td>
<td>CM</td><td>CM</td><td>CM</td><td>CM</td><td>CM</td><td>CM</td><td>(H</td><td>rH</td><td></td><td>rH</td>
<td>fe</td><td>fe</td><td></td><td>t</td><td></td><td>•s</td><td>fe</td><td>fe</td><td></td><td>fe</td>
<td>r-</td><td>r</td><td>r-</td><td></td><td></td><td>r*</td><td>Γ-</td><td>r-</td><td></td><td>r-</td>
<td>fe</td><td>fe</td><td>fe</td><td></td><td>fe</td><td>fe</td><td>fe</td><td>fe</td><td></td><td>fe</td>
<td>«—fe</td><td></td><td>«—fe</td><td> «—^</td><td>--fe</td><td>«—fe</td><td>«—fe</td><td>«-fe,</td><td></td><td> «^</td>
<td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>a</td><td>X</td><td>ac</td><td></td><td>3C</td>
<td>rH</td><td>rH</td><td>rH</td><td>j</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td><td></td><td>rH</td>
<td>fe</td><td></td><td>fe</td><td>fe</td><td>fe</td><td>fe</td><td>fe</td><td>fe</td><td></td><td>fe</td>
<td>ε</td><td>e</td><td>ε</td><td>ε</td><td>ε</td><td>ε</td><td>ε</td><td>ε</td><td></td><td>ε</td>
<td></td><td> ·*—*</td><td>fe—*</td><td>fe“*</td><td>fe—*</td><td>fe-*</td><td>fe-*</td><td>fe—*</td><td></td><td>fe—'</td>
<td>r-</td><td>r-</td><td>r-</td><td>r-</td><td>r-</td><td>r—</td><td>o</td><td>o</td><td></td><td> 0</td>
<td>CM</td><td>CM</td><td>CM</td><td>CM</td><td>CM</td><td>CM</td><td>cn</td><td>cn</td><td></td><td>σι</td>
<td></td><td>fe</td><td>fe</td><td>fe</td><td>fe</td><td>fe</td><td>fe</td><td>fe</td><td></td><td> *»</td>
<td>VO</td><td>LO</td><td>LO</td><td>LO</td><td>LO</td><td>vo</td><td>LO</td><td>vo</td><td></td><td>LO</td>
<td>fe</td><td>fe</td><td>fe</td><td></td><td>fe</td><td>fe</td><td>fe</td><td>fe</td><td></td><td>fe</td>
<td>«—fe</td><td> «—».</td><td></td><td>«—fe</td><td>—-fe</td><td>«—fe</td><td>«—fe.</td><td>«—fe</td><td></td><td>«—fe</td>
<td>X</td><td>X</td><td>X</td><td>X</td><td></td><td>X</td><td>X</td><td>ne</td><td></td><td>X</td>
<td>rH</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td><td></td><td>rH</td>
<td></td><td>fe</td><td>fe</td><td></td><td>fe</td><td>fe</td><td>fe</td><td>fe</td><td></td><td>fe</td>
<td>ε</td><td>S</td><td>e</td><td>ε</td><td>ε</td><td>ε</td><td>e</td><td>e</td><td></td><td>ε</td>
<td>fe—·</td><td>fe—*</td><td>fe—*</td><td></td><td>fe-*</td><td>fe-—</td><td>fe—*</td><td>fe—·</td><td>CM</td><td>fe—*</td>
<td>o</td><td>o</td><td>co</td><td>co</td><td>PO</td><td>PO</td><td>r-~</td><td> 0-</td><td>LO</td><td> 0</td>
<td>cn</td><td>cn</td><td>cn</td><td>cn</td><td>cn</td><td>cn</td><td>r-</td><td>r-~</td><td></td><td>co</td>
<td></td><td></td><td>χ</td><td>fe</td><td> ·.</td><td></td><td>fe</td><td>fe</td><td>O</td><td>fe</td>
<td>LO</td><td>LO</td><td>LO</td><td>LO</td><td>LO</td><td>UO</td><td>LO</td><td>LO</td><td>LO</td><td>LO</td>
<td>CM</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td>
<td> 1</td><td> 1</td><td> 1</td><td> 1</td><td> 1</td><td> 1</td><td>CM</td><td> 1</td><td> 1</td>
<td>CO</td><td>fe</td><td>fe</td><td>fe</td><td>fe</td><td>fe</td><td> 1</td><td>fe</td><td>fe</td>
<td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td>
<td>iŪ</td><td> 1</td><td>Ί</td><td> 1</td><td>Ί</td><td> 1</td><td>CO</td><td> 1</td><td> 1</td>
<td>rH</td><td></td><td></td><td></td><td></td><td></td><td>(Ū</td><td></td><td></td>
<td>•H</td><td></td><td></td><td></td><td></td><td></td><td>H</td><td></td><td></td>
<td>q</td><td></td><td></td><td></td><td></td><td></td><td>•H</td><td></td><td></td>
<td> 0</td><td></td><td></td><td></td><td></td><td></td><td>C</td><td></td><td></td>
<td>G</td><td></td><td></td><td></td><td></td><td></td><td>Q)</td><td></td><td></td>
<td> 3</td><td></td><td></td><td></td><td></td><td></td><td>•H</td><td></td><td></td>
<td>X</td><td></td><td></td><td></td><td></td><td></td><td> 4-></td><td></td><td></td>
£
I
Ό 'č?
X
X lentelė •y
CM
Cx x
i
II s
X
I
<td colspan="2">PO 1</td><td> 1</td><td colspan="2">(Ū rH</td><td colspan="3">PO 1</td><td colspan="2"> 1</td>
<td> 0</td><td></td><td> 0</td><td></td><td>•H</td><td></td><td> 0</td><td></td><td>co</td><td></td>
<td><Ū</td><td></td><td>IŪ</td><td></td><td>c</td><td></td><td>iū</td><td></td><td><ū</td><td></td>
<td>Ή</td><td></td><td>rH</td><td></td><td>iŪ</td><td></td><td>rH</td><td></td><td>Ή</td><td></td>
<td>-H</td><td></td><td>•H</td><td></td><td>G</td><td></td><td>•H</td><td></td><td>Ή</td><td></td>
<td>c</td><td></td><td>c</td><td></td><td>•H</td><td></td><td>G</td><td></td><td>c</td><td></td>
<td>iū</td><td></td><td>>V</td><td> 1</td><td>CM</td><td> 1</td><td>iū</td><td> 1</td><td>(ū</td><td> 1</td>
<td>G -H</td><td>Ί</td><td>G •H</td><td>Ί</td><td>0 •H</td><td>Ί</td><td>G •H</td><td>Ί</td><td>G •H</td><td></td>
<td>CM</td><td></td><td>CM</td><td></td><td>X</td><td></td><td>CM</td><td></td><td>CM</td><td></td>
<td>O</td><td></td><td> 0</td><td></td><td> 0</td><td></td><td>O</td><td></td><td>O</td><td></td>
<td>G</td><td></td><td>G</td><td></td><td>G</td><td></td><td>G</td><td></td><td>G</td><td></td>
<td>T)</td><td></td><td>X</td><td></td><td>TJ</td><td></td><td>T</td><td></td><td>Ti</td><td></td>
<td>-H</td><td></td><td>• H</td><td></td><td>•H</td><td></td><td>•H</td><td></td><td>-H</td><td></td>
<td>X</td><td></td><td>H</td><td></td><td>X</td><td></td><td>X</td><td></td><td>X</td><td></td>
<td> 0</td><td></td><td> 0</td><td></td><td> 0</td><td></td><td>iū</td><td></td><td>(ū</td><td></td>
<td>G</td><td></td><td>G</td><td></td><td>G</td><td></td><td>G</td><td></td><td>G</td><td></td>
<td>X</td><td></td><td>4J</td><td></td><td>X</td><td></td><td>X</td><td></td><td>X</td><td></td>
<td> 0</td><td></td><td> 0</td><td></td><td> 0</td><td></td><td> 0</td><td></td><td> 0</td><td></td>
<td>X</td><td></td><td>-U</td><td></td><td>X</td><td></td><td>X</td><td></td><td>X</td><td></td>
<td></td><td>CO</td><td></td><td> 0</td><td></td><td>CO</td><td></td><td>CO</td><td></td><td>co</td>
<td></td><td>(Ū</td><td></td><td><Ū</td><td></td><td>iŪ</td><td></td><td> 0</td><td></td><td> 0</td>
<td> 0</td><td>rH</td><td>CO</td><td>rH</td><td> 0</td><td>Ή</td><td> 0</td><td>r—j</td><td> 0</td><td>rH</td>
<td><Ū</td><td>• H</td><td><Ū</td><td>• H</td><td>iū</td><td>•H</td><td>fŪ</td><td>•H</td><td><Ū</td><td>•H</td>
<td>rH</td><td>Cm</td><td><H</td><td>CM</td><td>Ή</td><td>CM</td><td>rH</td><td>CM</td><td>rH</td><td>o,</td>
<td>•H</td><td> 0</td><td>H</td><td>O</td><td>•H</td><td> 0</td><td>Ή</td><td>O</td><td>•H</td><td> 0</td>
<td>X</td><td>G</td><td>X</td><td>G</td><td>X</td><td>G</td><td>X</td><td>G</td><td>X</td><td>G</td>
<td> 0</td><td>CM</td><td> 0</td><td>CM</td><td> 0</td><td>CM</td><td> 0</td><td>CM</td><td> 0</td><td>CM</td>
<td>rH</td><td>X</td><td>X</td><td></td><td>X</td><td>LO</td><td>Γ</td><td> 00</td><td>cn</td><td>O</td>
<td>O</td><td> 0</td><td>o</td><td> 0</td><td> 0</td><td> 0</td><td>o</td><td> 0</td><td> 0</td><td>rH</td>
<td>rH</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td>
<td>iH</td><td> «—1</td><td>rH</td><td>»H</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td>
11.11 etilas tetrahidrotiopiranilas-3 - 6,80(m,IH), 6, 90(m,IH) , 7,10(m,IH)
<td>X rH</td><td>X rH</td><td>X rH</td><td>X rH</td><td>X rH</td><td>X rH</td><td>X rH</td>
<td>χ</td><td>X</td><td>X</td><td></td><td>K</td><td>X</td><td>X</td>
<td>e</td><td> £</td><td> £</td><td> £</td><td> £</td><td> £</td><td>i£</td>
<td>-χ-''</td><td>X—r</td><td>—r</td><td>X—r·</td><td>•Χχ·»'</td><td></td><td></td>
<td>o</td><td>cn</td><td> 00</td><td>cn</td><td>cn</td><td>o</td><td>O</td>
<td>r—J</td><td>X</td><td>LT)</td><td>LO</td><td>LD</td><td>LD</td><td>LD</td>
<td>x</td><td>X</td><td>X</td><td>x</td><td>x</td><td>χ</td><td>X</td>
<td>r*-</td><td>kO</td><td>kO</td><td>kO</td><td>kO</td><td>kO</td><td>LD</td>
<td>x</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td>
<td>x</td><td>X</td><td>>—X</td><td>X-X</td><td></td><td>^-X</td><td>^-X</td>
<td>X</td><td>K</td><td>X</td><td>K</td><td>K</td><td>ru</td><td>X</td>
<td>rH</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td>
<td>x</td><td>X</td><td>X</td><td>X</td><td>χ</td><td>X</td><td>X</td>
<td> £</td><td> £</td><td> £</td><td>s</td><td>e</td><td>e</td><td> £</td>
<td>-—τ'</td><td>-—r</td><td>'—r</td><td>•X—'</td><td>χ—·</td><td>χ—»·</td><td>x«—·</td>
<td>O</td><td>kO</td><td>kO</td><td>kO</td><td>kO</td><td>kO</td><td>kO</td>
<td>o</td><td>o</td><td>o</td><td>o</td><td>o</td><td>o</td><td>o</td>
<td>X</td><td>X</td><td>x</td><td>x</td><td>x</td><td>>x</td><td>X</td>
<td>kO</td><td>kO</td><td>kO</td><td>kO</td><td>kO</td><td>kO</td><td>kO</td>
<td>χ</td><td>x</td><td>x</td><td></td><td>X</td><td>X</td><td>X</td>
<td>>—X</td><td>X</td><td>X</td><td>Χ—Χ.</td><td>,^-χ</td><td>,—χ</td><td>^χ.</td>
<td>X</td><td>ru</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td>
<td>t—1</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td>
<td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>X</td>
<td> £</td><td> £</td><td> £</td><td> £</td><td> £</td><td> £</td><td> £</td>
<td>•—τ'</td><td></td><td></td><td>'—•r</td><td>X—··'</td><td>X—·</td><td>X—*·</td>
<td>o</td><td>O</td><td>o</td><td>r^~</td><td>r^·</td><td>o</td><td>o</td>
<td> 00</td><td><n</td><td>0Ί</td><td> 00</td><td>co</td><td>σ\</td><td>cn</td>
<td>X</td><td>X</td><td>X</td><td>X</td><td>X</td><td>x</td><td>X</td>
<td>kO</td><td>kO</td><td>kO</td><td>LO</td><td>kO</td><td>kO</td><td>LD</td>
CM
I
CO (O
UI (fl
I—I •H α
o μ
CL
CM o
μ •rd a
•rd
X i i i
Ί 'ι Ί i
'1 η
i cn
<td colspan="2"> 00 1</td><td colspan="2">’T 1</td><td colspan="2">ίϋ rH</td>
<td>W</td><td></td><td>cn</td><td></td><td>Ή</td><td></td>
<td><T3</td><td></td><td>n5</td><td></td><td>c</td><td></td>
<td>rH</td><td></td><td>rH</td><td></td><td>(fl</td><td></td>
<td>•H</td><td></td><td>•H</td><td></td><td>μ</td><td></td>
<td>C</td><td></td><td>c</td><td></td><td>μ</td><td></td>
<td></td><td>I</td><td>(fl</td><td> 1</td><td>CL</td><td> 1</td>
<td>u</td><td> -</td><td>μ</td><td> -</td><td>o</td><td> -</td>
<td>• H</td><td>l</td><td>•H</td><td>Ί</td><td>•H</td><td>Ί</td>
<td>α</td><td></td><td>CL</td><td></td><td>X</td><td></td>
<td> 0</td><td></td><td>O</td><td></td><td>o</td><td></td>
<td>μ</td><td></td><td>μ</td><td></td><td>μ</td><td></td>
<td>t</td><td></td><td>t</td><td></td><td>X</td><td></td>
<td>•H</td><td></td><td>•rd</td><td></td><td>•H</td><td></td>
<td>X</td><td></td><td>X</td><td></td><td>cU</td><td></td>
<td>(fl</td><td></td><td> <0</td><td></td><td>rū</td><td></td>
<td>μ</td><td></td><td>μ</td><td></td><td>M</td><td></td>
<td>X</td><td></td><td>X</td><td></td><td>-P</td><td></td>
<td>Φ</td><td></td><td>(D</td><td></td><td>(D</td><td></td>
<td>X</td><td></td><td>X</td><td></td><td>-P</td><td></td>
<td>fn</td><td>cn Π3 rH</td><td>cn</td><td>cn (fl X</td><td>cn</td><td>cn OJ rH</td>
<td>(ΰ</td><td>•H</td><td>(fl</td><td>μ</td><td>(Ū</td><td>•H</td>
<td>rH</td><td>CU</td><td>i-f</td><td>CL</td><td>rH</td><td>CL</td>
<td>-H</td><td>o</td><td>μ</td><td>O</td><td>•H</td><td>O</td>
<td>P</td><td>M</td><td>X</td><td>μ</td><td>-P</td><td>μ</td>
<td></td><td>et</td><td> <1)</td><td>CL</td><td> 0)</td><td>CL</td>
<td>OO</td><td>*T</td><td>LD</td><td>LD</td><td> 1^·</td><td>co</td>
<td>rH</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td><td>H</td>
<td>rH</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td>
<td>rH</td><td>rH</td><td>rH</td><td>rH</td><td>rH</td><td>H</td>
Application examples
The effect of cyclohexenone derivatives of formula I on plant growth can be demonstrated by tests in a greenhouse.
For plant cultivation plastic cups were used for flower cultivation, which were filled with sandy and 3% humus substrate. The seeds of the test plants are sown separately by species.
For pre-emergence treatment, biologically active substances emulsified or suspended in water are sprayed with a fine spray immediately after sowing. The dishes are watered sparingly, covered with a translucent plastic wrap before the plants grow, to encourage germination and growth, as the biologically active substance does not harm.
Biologically active substances suspended or emulsified in water are used in the treatment of test plants after germination at a height of 3 to 15 cm. For this purpose, 0.25 kg / ha of biologically active substances is used.
The plants are stored at 10-15 ° C or 20-35 ° C, depending on their species. The duration of the experiment is 2 to 4 weeks. During this time, the plants are monitored and their response to the different treatments is recorded.
A rating scale from 0 to 100. By the way, 100 means no plant sprouts or completely damaged parts of the soil surface, 0 means no damage or normal growth process.
Plants used in greenhouse tests for the following species:
Oryza sativa - rice
Setaria viridis is a green bristle
For post-emergence treatments using no. 8.08 allowed effective control of unwanted herbaceous plants without damaging rice grown as a test crop.
Results of Formula I for confirmation of the effect of cyclohexenone oxime below. The weed control agents contained 100 g of active active compound in 1 liter, consisting of 93 IU. % xylene and 7 wt. % lutenzol AP 8 (moisturizing with emulsifying and dispersing action, based on eight times ethoxylated nonylphenol).
ethers herbicide provided test
TABLE I
The rate of application is 0.5 kg / ha of active material after germination
<td>Compound No.</td><td>Violation of Echinochloa (%)</td>
<td> 5, 06</td><td> 85</td>
<td> 5,08</td><td> 95</td>
<td> 5, 16</td><td> 70</td>
<td> 5, 18</td><td> 70</td>
<td> 6, 09</td><td> 70</td>
<td> 6, 10</td><td> 70</td>
<td> 6, 12</td><td> 70</td>
<td> 6,14</td><td> 70</td>
<td> 6,16</td><td> 98</td>
continuation of the table
ΊΟ
<td>Compound No.</td><td>Violation of Echinochloa (%)</td>
<td> 6,18</td><td> 90</td>
<td> 7,13</td><td> 95</td>
<td> 7,14</td><td> 95</td>
<td> - 7,15</td><td> 98</td>
<td> 7, 16</td><td> 95</td>
<td> 7, 17</td><td> 90</td>
<td> 7, 18</td><td> 98</td>
<td> 8, 08</td><td> 65</td>
<td> 8,09</td><td> 70</td>
<td> 8,10</td><td> 75</td>
<td> 10, 08</td><td> 85</td>
<td> 10, 12</td><td> 70</td>
<td>TABLE 2</td><td></td>
<td>Consumption rate</td><td>0.5 kg / ha of active substance,</td>
pre-emergence treatment
<td>Compound No.</td><td>Violation of Echinochloa (%)</td>
<td> 4,10</td><td> 65</td>
<td> 5, 08</td><td> 90</td>
<td> 6, 06</td><td> 85</td>
<td> 6, 24</td><td> 90</td>
<td> 7,17</td><td> 75</td>
<td> 7,20</td><td> 80</td>
<td> 7, 22</td><td> 90</td>
<td> 7,24</td><td> 70</td>
continuation of the table
<td>Compound No.</td><td>Infringement</td><td>Echinochloa</td><td> (%)</td>
<td> 7,27</td><td></td><td> 75</td><td></td>
<td> 8,05</td><td></td><td> 65</td><td></td>
<td> 8,18</td><td></td><td> 65</td><td></td>
<td> 8,20</td><td></td><td> 75</td><td></td>
<td> 8,21</td><td></td><td> 65</td><td></td>
<td> 8, 30</td><td></td><td> 75</td><td></td>
<td> 8, 31</td><td></td><td> 75</td><td></td>
<td> 8,32</td><td></td><td> 85</td><td></td>
<td> 8,33</td><td></td><td> 80</td><td></td>
<td> 8, 39</td><td></td><td> 65</td><td></td>
<td> 10, 07</td><td></td><td> 75</td><td></td>
<td> 11,08</td><td></td><td> 70</td><td></td>
<td>TABLE 3</td><td></td><td></td><td></td>
<td>Consumption rate post-emergence treatment</td><td colspan="3">0.5 kg / ha of active substance,</td>
<td>Compound No.</td><td>Violation Lolium</td><td>multiflorum</td><td> (%)</td>
<td> 2,10</td><td> 80</td><td></td><td></td>
<td> 2,12</td><td> 70</td><td></td><td></td>
<td> 3, 16</td><td> 80</td><td></td><td></td>
<td> 5, 02</td><td> 95</td><td></td><td></td>
<td> 5,10</td><td> 85</td><td></td><td></td>
<td> 5,12</td><td> 70</td><td></td><td></td>
<td> 5,24</td><td> 98</td><td></td><td></td>
<td> 6, 07</td><td> 80</td><td></td><td></td>
continuation of the table
<td>Compound No.</td><td>Damage to Lolium multiflorum (%)</td>
<td> 6,08</td><td> 80</td>
<td> 6, 09</td><td> 70</td>
<td> 6,10</td><td> 80</td>
<td></td><td></td>
<td> 6,14 </td><td> 70</td>
<td> 8,26</td><td> 65</td>
<td> 8, 29</td><td> 70</td>
TABLE
Application rate 0.5 kg / ha of active substance after germination treatment
<td rowspan="2">Compound No.</td><td colspan="2">Plants examined and degree of damage,%</td>
<td>Echinochloa</td><td>Lolium multiflorum</td>
<td> 3,10</td><td> 70</td><td> 70</td>
<td> 4,04</td><td> 95</td><td> 70</td>
<td> 4,16</td><td> 90</td><td> 70</td>
<td> 5, 28</td><td> 95</td><td> 85</td>
<td> 5,29</td><td> 70</td><td> 65</td>
<td> 5, 31</td><td> 90</td><td> 100</td>
<td> 6, 04</td><td> 90</td><td> 90</td>
<td> 6, 16</td><td> 70</td><td> 80</td>
<td> 6,19</td><td> 100</td><td> 100</td>
<td> 6,20</td><td> 90</td><td> 100</td>
<td> 6,21</td><td> 90</td><td> 95</td>
<td> 6,22</td><td> 100</td><td> 100</td>
continuation of the table
<td rowspan="2">Compound No.</td><td colspan="3">Plants examined and degree of damage,%</td>
<td>Echinochloa</td><td>Lolium</td><td>multiflorum</td>
<td> 6, 23</td><td> 90</td><td></td><td> 95</td>
<td> 7, 13</td><td> 85</td><td></td><td> 85</td>
<td> 7,14</td><td> 100</td><td></td><td> 98</td>
<td> 7, 15</td><td> 98</td><td></td><td> 75</td>
<td> 7, 16</td><td> 100</td><td></td><td> 100</td>
<td> 7, 18</td><td> 85</td><td></td><td> 95</td>
<td> 8,25</td><td> 65</td><td></td><td> 80</td>
<td> 8,27</td><td> 75</td><td></td><td> 100</td>
<td> 10, 08</td><td> 70</td><td></td><td> 95</td>
<td> 10, 09</td><td> 75</td><td></td><td> 75</td>
<td> 10,10</td><td> 80</td><td></td><td> 75</td>
Contents182
25 sheets
Sheet 1 Sheet 2 Sheet 3 Sheet 4 Sheet 5 Sheet 6 Sheet 7 Sheet 8 Sheet 9 Sheet 10 Sheet 11 Sheet 12 Sheet 13 Sheet 14 Sheet 15 Sheet 16 Sheet 17 Sheet 18 Sheet 19 Sheet 20 Sheet 21 Sheet 22 Sheet 23 Sheet 24 Sheet 25
Every citation, both ways
| Document | Relation | Office | Cited during |
|---|---|---|---|
| EP0080301A2 | Cites | European Patent Office (EPO) | Applicant |
| EP0125094A2 | Cites | European Patent Office (EPO) | Applicant |
| EP0137174A1 | Cites | European Patent Office (EPO) | Applicant |
| EP0142741A2 | Cites | European Patent Office (EPO) | Applicant |
| EP0177913A1 | Cites | European Patent Office (EPO) | Applicant |
| US4249937A | Cites | United States of America | Applicant |
22 members in 14 offices
Priority claims4
| Document | Office | Kind | Date |
|---|---|---|---|
| 4014987 | Germany | A | |
| 4014987 | Germany | A | |
| 40149870 | – | – | – |
| DE19904014987 | – | – | – |
Members22
| Document | Office | Kind | |
|---|---|---|---|
| CA2041794A1 | Canada | A1 | |
| EP0456118A2 | European Patent Office (EPO) | A2 | |
| DE4014987A1 | Germany | A1 | |
| HUT57006A | Hungary | A | |
| BR9101869A | Brazil | A | |
| KR910019994A | Republic of Korea | A | |
| JPH04225957A | Japan | A | |
| ZA913481B | South Africa | B | |
| EP0456118A3 | European Patent Office (EPO) | A3 | |
| US5228896A | United States of America | A | |
| US5330965A | United States of America | A | |
| LTIP526A | Lithuania | A | |
| LV10361A | Latvia | A | |
| LT3295BThis record | Lithuania | B | |
| LV10361B | Latvia | B | |
| HU212480B | Hungary | B | |
| RU2083577C1 | Russian Federation | C1 | |
| EP0456118B1 | European Patent Office (EPO) | B1 | |
| AT169624T | Austria | T | |
| ATE169624T1 | Austria | T1 | |
| DE59109039D1 | Germany | D1 | |
| UA27221C2 | Ukraine | C2 |
1 legal event, as the office reported them to INPADOC
Events
| Event | Code | |
|---|---|---|
| Lapsed patentsLapsedMM9A | MM9A |
Numbers
- Publication, DOCDB
- 3295
- Publication, EPODOC
- LT3295
- Application
- 526
- Application, DOCDB
- IP526
- Application, EPODOC
- LTIP526
Titles
- English
- CYCLOHEXENONOXIME ETHERS AND HERBICIDAL COMPOSITION
Classification
- CPC, 12
- C07D207/333
- C07D309/00
- A01N43/10
- A01N43/16
- A01N43/36
- A01N43/40
- C07D307/42
- C07D333/16
- C07D333/28
- C07D405/12
- C07D407/12
- C07D409/12
- IPC, 20
- A01N43 08
- A01N43 10
- A01N43 16
- A01N43 18
- A01N43 36
- A01N43 40
- A01P13 00
- C07D213 30
- C07D207 32
- C07D207 333
- C07D307 38
- C07D307 42
- C07D333 16
- C07D333 28
- C07D405 08
- C07D405 12
- C07D407 08
- C07D407 12
- C07D409 08
- C07D409 12