Issue 6, 1983
From the journal:

Journal of the Chemical Society, Chemical Communications

Stereoselectivity of prochiral thioalkyl groups in the enzymatic oxidation of thioacetals by fungi

Barbara J. Auret,   Derek R. Boyd,   E. Sally Cassidy,   Fiona Turley,   Alex F. Drake  and  Stephen F. Mason  

Abstract

Enzymatic oxidation of 2-substituted 1,3-dithians in cultures of a Helminthosporium species shows a stereoperference for equatorial oxidation and for (1S)-monosulphoxide products.

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Article information

DOI
https://doi.org/10.1039/C39830000282
Article type
Paper

J. Chem. Soc., Chem. Commun., 1983, 282-283

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Stereoselectivity of prochiral thioalkyl groups in the enzymatic oxidation of thioacetals by fungi

B. J. Auret, D. R. Boyd, E. S. Cassidy, F. Turley, A. F. Drake and S. F. Mason, J. Chem. Soc., Chem. Commun., 1983, 282 DOI: 10.1039/C39830000282

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