Issue 9, 1970

Homolytic substitution at tin by the succinimidyl radical

Abstract

N-Bromosuccinimide readily reacts with tetra-alkyltin compounds by a free-radical chain mechanism involving bimolecular homolytic substitution by the succinimidyl radical at tin in one of the propagation steps.

Article information

Article type
Paper

J. Chem. Soc. D, 1970, 557-558

Homolytic substitution at tin by the succinimidyl radical

A. G. Davies, B. P. Roberts and J. M. Smith, J. Chem. Soc. D, 1970, 557 DOI: 10.1039/C29700000557

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