Issue 22, 1983

Elaboration of α-substituted benzyl ethers and sulphides by suppression of the Wittig and related rearrangements

Abstract

Co-ordination of benzyl alkyl ethers and sulphides to chromium tricarbonyl allows α-substitution via the corresponding α-carbanions to be achieved by suppression of the Wittig and related rearrangements.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1983, 1316-1317

Elaboration of α-substituted benzyl ethers and sulphides by suppression of the Wittig and related rearrangements

S. G. Davies, N. J. Holman, C. A. Laughton and B. E. Mobbs, J. Chem. Soc., Chem. Commun., 1983, 1316 DOI: 10.1039/C39830001316

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