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US 2003/0119664 A1Published application
Chiral monophosphorus compounds
AssigneeBayer Aktiengesellschaft
InventorsClaus Dreisbach, Benjamin Meseguer, Thomas Prinz, Ulrich Scholz, Hans-Christian Militzer, Friederike Agel, Birgit Driessen-Holscher
Life of this patent
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Abstract
The present invention relates to catalysts comprising chiral monophosphorus compounds and their use, the chiral monophosphorus compounds themselves and also their precursors.
Claims25
Chiral monophosphorus compounds of the general formula (I),
- 14
- where
- R1 is an unsubstituted or substituted 1,1′-biphenyl-2,2′-diyl radical and
- R2 is a radical selected from the group consisting of substituted or unsubstituted alkyl, substituted or unsubstituted aryl, substituted or unsubstituted alkoxy, substituted or unsubstituted aryloxy and tertiary amino.
1 more element
Chiral monophosphorus compounds selected from the group consisting of
- (S)-5,5′-Dichloro-6,6′-dimethoxy-1,1′-biphenyl-2,2′-diyl isopropyl phosphite,
- (R)-5,5′-dichloro-6,6′-dimethoxy-1,1′-biphenyl-2,2′-diyl isopropyl phosphite,
- (R)-5,5′-dichloro-6,6′-dimethoxy-1,1′-biphenyl-2,2′-diyl (R)-1-phenylethyl phosphite,
- (R)-5,5′-dichloro-6,6′-dimethoxy-1,1′-biphenyl-2,2′-diyl (S)-1-phenylethyl phosphite,
- (S)-5,5′-dichloro-6,6′-dimethoxy-1,1′-biphenyl-2,2′-diyl (R)-1-phenylethyl phosphite,
- (S)-5,5′-dichloro-6,6′-dimethoxy-1,1′-biphenyl-2,2′-diyl (S)-1-phenylethyl phosphite,
- (S)-5,5′-dichloro-6,6′-dimethoxy-1,1′-biphenyl-2,2′-diyl cyclohexyl phosphite,
- (R)-5,5′-dichloro-6,6′-dimethoxy-1,1′-biphenyl-2,2′-diyl cyclohexyl phosphite,
- (S)-5,5′-dichloro-6,6′-dimethoxy-1,1′-biphenyl-2,2′-diyl phenyl phosphite,
- (R)-5,5′-dichloro-6,6′-dimethoxy-1,1′-biphenyl-2,2′-diyl phenyl phosphite,
- (S)-5,5′-dichloro-6,6′-dimethoxy-1,1′-biphenyl-2,2′-diyl 2,6-dimethylphenyl phosphite,
- (R)-5,5′-dichloro--6,6′-dimethoxy-1,1′-biphenyl-2,2′-diyl 2,6-dimethylphenyl phosphite,
- (S)-5,5′,6,6′-tetramethyl-3,3′-bis(tert-butyl)-1,1′-biphenyl-2,2′-diyl isopropyl phosphite,
- (R)-5,5′,6,6′-tetramethyl-3,3′-bis(tert-butyl)-1,1′-biphenyl-2,2′-diyl isopropyl phosphite,
- (S)-5,5′,6,6′-tetramethyl-3,3′-bis(tert-butyl)-1,1′-biphenyl-2,2′-diyl (rac)-1-phenylethyl phosphite,
- (R)-5,5′,6,6′-tetramethyl-3,3′-bis(tert-butyl)-1,1′-biphenyl-2,2′-diyl (rac)-1-phenylethyl phosphite,
- (S)-5,5′,6,6′-tetramethyl-3,3′-bis(tert-butyl)-1,1′-biphenyl-2,2′-diyl (S)-1-phenylethyl phosphite,
- (R)-5,5′,6,6′-tetramethyl-3,3′-bis(tert-butyl)-1,1′-biphenyl-2,2′-diyl (S)-1-phenylethyl phosphite,
- (S)-5,5′,6,6′-tetramethyl-3,3′-bis(tert-butyl)-1,1′-biphenyl-2,2′-diyl (R)-1-phenylethyl phosphite,
- (R)-5,5′,6,6′-tetramethyl-3,3′-bis(tert-butyl)-1,1′-biphenyl-2,2′-diyl (R)-1-phenylethyl phosphite,
- (S)-5,5′,6,6′-tetramethyl-3,3′-bis(tert-butyl)-1,1′-biphenyl-2,2′-diyl diphenylmethyl phosphite,
- (R)-5,5′,6,6′-tetramethyl-3,3′-bis(tert-butyl)-1,1′-biphenyl-2,2′-diyl diphenylmethyl phosphite,
- (S)-5,5′,6,6′-tetramethyl-3,3′-bis(tert-butyl)-1,1′-biphenyl-2,2′-diyl methyl phosphite,
- (R)-5,5′,6,6′-tetramethyl-3,3′-bis(tert-butyl)-1,1′-biphenyl-2,2′-diyl methyl phosphite,
- (S)-5,5′,6,6′-tetramethyl-3,3′-bis(tert-butyl)-1,1′-biphenyl-2,2′-diyl 2,6-dimethylphenyl phosphite,
- (R)-5,5′,6,6′-tetramethyl-3,3′-bis(tert-butyl)-1,1′-biphenyl-2,2′-diyl 2,6-dimethylphenyl phosphite,
- (S)-5,5′,6,6′-tetramethyl-3,3′-bis(tert-butyl)-1,1′-biphenyl-2,2′-diyl 2,6-diisopropylphenyl phosphite,
- (R)-5,5′,6,6′-tetramethyl-3,3′-bis(tert-butyl)-1,1′-biphenyl-2,2′-diyl 2,6-diisopropylphenyl phosphite,
- (S)-5,5′,6,6′-tetramethyl-3,3′-bis(tert-butyl)-1,1′-biphenyl-2,2′-diyl phenyl phosphite,
- (R)-5,5′,6,6′-tetramethyl-3,3′-bis(tert-butyl)-1,1′-biphenyl-2,2′-diyl phenyl phosphite,
- (S)-5,5′,6,6′-tetramethyl-3,3′-bis(tert-butyl)-1,1′-biphenyl-2,2′-diyl ethyl phosphite,
- (R)-5,5′,6,6′-tetramethyl-3,3′-bis(tert-butyl)-1,1′-biphenyl-2,2′-diyl ethyl phosphite
- (S)-5,5′,6,6′-tetramethyl-3,3′-bis(tert-butyl)-1,1′-biphenyl-2,2′-diyl 4-tert-butylphenyl phosphite and
- (R)-5,5′,6,6′-tetramethyl-3,3′-bis(tert-butyl)-1,1′-biphenyl-2,2′-diyl 4-tert-butylphenyl phosphite.
31 more elements
Compounds of the general formula (XI)
- 18
- where R1 is an unsubstituted or substituted 1,1′-biphenyl-2,2′-diyl radical and
- Akt is chlorine, bromine, iodine or dialkylamino.
Catalysts comprising transition metal complexes of chiral monophosphorus compounds of the general formula (I),
- 19
- where
- R1 is an unsubstituted or substituted 1,1′-biphenyl-2,2′-diyl radical and
- R2 is a radical selected from the group consisting of substituted or unsubstituted alkyl, substituted or unsubstituted aryl, substituted or unsubstituted alkoxy, substituted or unsubstituted aryloxy and tertiary amino.
1 more element
Dependencies are inferred from the claim text.