Issue 16, 1991

Enzymatic preparation of enantiomerically pure and selectively protected 1,2- and 1,3-diols

Abstract

The optically pure, selectively protected 1,2- and 1,3-diol derivatives (R)- and (S)-1–8 have been prepared by enzymatic hydrolysis of their racemic acetates and chloroacetates in the presence of ester hydrolase from Pseudomonas fluorescens(SAM-1).

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1991, 1066-1068

Enzymatic preparation of enantiomerically pure and selectively protected 1,2- and 1,3-diols

U. Goergens and M. P. Schneider, J. Chem. Soc., Chem. Commun., 1991, 1066 DOI: 10.1039/C39910001066

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