Issue 3, 1986

Stereochemistry of intramolecular homolytic substitution at the sulphur atom of a chiral sulphoxide

Abstract

The formation of the cyclic sulphoxide (R)-(6) by treatment of the bromoarene (R)-(2) with tributylstannane indicates that intramolecular homolytic substitution at the sulphur centre of the sulphoxide group proceeds with strict inversion of configuration.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1986, 189-190

Stereochemistry of intramolecular homolytic substitution at the sulphur atom of a chiral sulphoxide

A. L. J. Beckwith and D. R. Boate, J. Chem. Soc., Chem. Commun., 1986, 189 DOI: 10.1039/C39860000189

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