Homolytic substitution at tin by the succinimidyl radical
- 1 January 1970
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society D: Chemical Communications
- No. 9,p. 557-558
- https://doi.org/10.1039/c29700000557
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.Keywords
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