Nova Patents
AT211479T

Chiral ferrocenyls

Abstract

The invention relates to compounds of formula (I) wherein R1 is alkyl, cycloalkyl or optionally substituted phenyl; Ra-P (R 10 R 11) or -SR 12; R10-R12, -CH2-NH-R12, -CH2-O-P (R10 R11), R10 and R11 are optionally substituted alkyl, or R 10 and R 11 together form an optionally substituted alkylated alkylene; R'10 and R11 are the same as R10 and R11, with the proviso that -P (R10R11) is a non-identity of -P (R11R11); R12 is hydrogen, optionally alkyl, cycloalkyl or phenyl; R'12 is the same as R12, with the proviso that -SR12 is not the same as SR112; Y-OR13, -SR14 or -NR15R16; R13hidrogénatom, alkyl (C 1 -C 18) alkylcarbonyl or, optionally substituted phenyl; R14 is hydrogen, alkyl optionally substituted phenyl; R15 and R16 are optionally unsubstituted and / or substituted with one or more heteroatoms, arylene or carbocyclic groups; or -NR15R16cyclic amine; with the proviso that R1 represents a methyl group, and Y is other than dimethylamino when it is diphenylphosphino and Rb is di-tert-butylphosphino, or Ra is di-tert-butyl ) -phosphino group and Rb is diphenylphosphino group. The compounds of the present invention can be used as enantioselective reactions as ligands of transition metal catalysts. ŕ alkyl optionally substituted phenyl; R15 and R16 are optionally unsubstituted and / or substituted with one or more heteroatoms, arylene or carbocyclic groups; or -NR15R16cyclic amine; with the proviso that R1 represents a methyl group, and Y is other than dimethylamino when it is diphenylphosphino and Rb is di-tert-butylphosphino, or Ra is di-tert-butyl ) -phosphino group and Rb is diphenylphosphino group. The compounds of the present invention can be used as enantioselective reactions as ligands of transition metal catalysts. ŕ alkyl optionally substituted phenyl; R15 and R16 are optionally unsubstituted and / or substituted with one or more heteroatoms, arylene or carbocyclic groups; or -NR15R16cyclic amine; with the proviso that R1 represents a methyl group, and Y is other than dimethylamino when it is diphenylphosphino and Rb is di-tert-butylphosphino, or Ra is di-tert-butyl ) -phosphino group and Rb is diphenylphosphino group. The compounds of the present invention can be used as enantioselective reactions as ligands of transition metal catalysts. ŕ with the proviso that R1 represents a methyl group, and Y is other than dimethylamino when it is diphenylphosphino and Rb is di-tert-butylphosphino, or Ra is di-tert-butyl ) -phosphino group and Rb is diphenylphosphino group. The compounds of the present invention can be used as enantioselective reactions as ligands of transition metal catalysts. ŕ with the proviso that R1 represents a methyl group, and Y is other than dimethylamino when it is diphenylphosphino and Rb is di-tert-butylphosphino, or Ra is di-tert-butyl ) -phosphino group and Rb is diphenylphosphino group. The compounds of the present invention can be used as enantioselective reactions as ligands of transition metal catalysts. ŕ

Term

No projected expiry on record.

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26 members in 14 offices

This recordMember, by publication datePriority claim4 more offices are in the list below

Priority claims3

Priority claims
DocumentOfficeKindDate
244096SwitzerlandA
244196SwitzerlandA
9705480European Patent Office (EPO)W

Members26

Family members, oldest first
DocumentOfficeKind
CA2263715A1CanadaA1
WO9815565A1World Intellectual Property Organization (WIPO)A1
AU4944197AAustraliaA
CZ117899A3CzechiaA3
EP0929560A1European Patent Office (EPO)A1
BR9712273ABrazilA
IL129329D0IsraelD0
HU9904186A2HungaryA2
HUP9904186A2HungaryA2
KR20000048802ARepublic of KoreaA
US6133464AUnited States of AmericaA
JP2001501638AJapanA
HU9904186A3HungaryA3
HUP9904186A3HungaryA3
EP0929560B1European Patent Office (EPO)B1
AT211479TThis recordAustriaT
ATE211479T1AustriaT1
DE69709883D1GermanyD1
ES2170942T3SpainT3
DE69709883T2GermanyT2
IL129329AIsraelA
CZ292412B6CzechiaB6
HU222691B1HungaryB1
KR100534190B1Republic of KoreaB1
CA2263715CCanadaC
JP4043051B2JapanB2