Issue 22, 1991

The stereochemical course of substitution at sulphur in a sulphite diester

Abstract

A single diastereoisomer of phenyl epiandrosterone sulphite and the single diastereoisomer of benzyl epiandrosterone sulphite derived from it by nucleophilic substitution with benzyl alcohol have both been shown by X-ray crystallographic analysis to have the Rs configuration and hence the reaction proceeds with inversion at sulphur.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1991, 1597-1598

The stereochemical course of substitution at sulphur in a sulphite diester

C. L. L. Chai, V. Humphreys, K. Prout and G. Lowe, J. Chem. Soc., Chem. Commun., 1991, 1597 DOI: 10.1039/C39910001597

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