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- W2085665058 abstract "New optically active β-amino alcohols, derived from various acyclic and cyclic amino acids with alkyl groups on the carbinol carbon atom, were used in the enantioselective reduction of prochiral ketones. The attachment of alkyl groups to the nitrogen atom of the catalyst (R)-1b was shown to influence favorably the enantioselectivity of the addition of diethylzinc to benzaldehyde. In both cases the resulting secondary alcohols were obtained in moderate to high optical yields." @default.
- W2085665058 created "2016-06-24" @default.
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- W2085665058 date "2010-08-04" @default.
- W2085665058 modified "2023-09-26" @default.
- W2085665058 title "ChemInform Abstract: New β-Amino Alcohols as Chiral Ligands for the Catalytic Enantioselective Reduction of Prochiral Ketones and the Nucleophilic Addition of Diethylzinc to Benzaldehyde." @default.
- W2085665058 cites W2949581322 @default.
- W2085665058 doi "https://doi.org/10.1002/chin.199638043" @default.
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