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Issue 22, 1983
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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.

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Article type: Paper
DOI: 10.1039/C39830001316
Citation: J. Chem. Soc., Chem. Commun., 1983,0, 1316-1317
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    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, 0, 1316
    DOI: 10.1039/C39830001316

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