Issue 17, 1986

A powerful new stereo-controlled method for epoxidation of electrophilic alkenes

Abstract

t-Butyl hydroperoxide and an alkyl-lithium in dry tetrahydrofuran are shown to epoxidise α,β-unsaturated esters and sulphones efficiently in a stereo- and regio-specific manner, while esters of chiral alcohols undergo diastereofacially selective epoxidation.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1986, 1378-1380

A powerful new stereo-controlled method for epoxidation of electrophilic alkenes

C. Clark, P. Hermans, O. Meth-Cohn, C. Moore, H. C. Taljaard and G. van Vuuren, J. Chem. Soc., Chem. Commun., 1986, 1378 DOI: 10.1039/C39860001378

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