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• W2043054191 abstract "Component B lipase of the Candida antarctica yeast displays high enantioselectivity in catalysing transesterification reactions in non-aqeuous media with chiral secondary alcohols. This was exploited to resolve racemates of 1-(pyridinyl)-ethanols, 1- (6-bromopyridin-2-yl)ethanol, and 1-(6-bromopyridin-2-yl)-2,2-dimethylpropanol. The lipase esterified the (R)-alcohols of the first four substrates in > -99% enantiomeric excess in less than three hours with 30–40% isolated yield. Remaining (S)-enantiomers were isolated in similar yields and in 97–98% ee. 1-(6-Bromopyridin-2-yl)-2,2-dimethylpropanol did not form any detectable ester in one week." @default.
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• W2043054191 date "1994-07-01" @default.
• W2043054191 modified "2023-09-30" @default.
• W2043054191 title "Preparation of 1-pyridinylethanols of high enantiomeric purity by lipase catalysed transesterifications" @default.
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• W2043054191 doi "https://doi.org/10.1016/0957-4166(94)80178-9" @default.
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