Issue 16, 1989

Product enantioselectivity of the microsomal and cytosolic epoxide hydrolase catalysed hydrolysis of meso epoxides

Abstract

1,2-Epoxycycloalkanes from C5 to C8 and cis-stilbene oxide are respectively hydrolysed to the corresponding (–)-(R,R)-trans-diols and to (+)-(R,R)-1,2-diphenylethane-1,2-diol by both the microsomal and the cytosolic epoxide hydrolase of rabbit liver, the former enzyme being more active and giving higher enantiomeric excesses.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1989, 1170-1171

Product enantioselectivity of the microsomal and cytosolic epoxide hydrolase catalysed hydrolysis of meso epoxides

G. Bellucci, I. Capitani, C. Chiappe and F. Marioni, J. Chem. Soc., Chem. Commun., 1989, 1170 DOI: 10.1039/C39890001170

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