Enzymic preparation of enantiomerically pure secondary alcohols. Ester synthesis by irreversible acyl transfer using a highly selective ester hydrolase from Pseudomonas sp.; an attractive alternative to ester hydrolysis
- 1 January 1988
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Chemical Communications
- No. 22,p. 1459-1461
- https://doi.org/10.1039/c39880001459
Abstract
A series of secondary alcohols [(R)- and (S)-(1)–(3) and (5)–(9)] of interest as attractive chiral auxiliaries were prepared in high chemical and optical yields via enzymic esterification under essentially anhydrous conditions by employing a highly selective ester hydrolase from Pseudomonas sp. and vinyl acetate as acyl donor.Keywords
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