Issue 17, 1986

Radical reactions in synthesis: carbon–carbon bond formation from 2-substituted allyl trialkyl stannanes

Abstract

A competing 1,3-rearrangement of allyl stannanes has been demonstrated to occur under the normal thermal homolytic allyl transfer reaction conditions which limits the substitution patterns in these processes; two methacrylyl stannanes are described which allow the transfer of the methacrylyl moiety to alkyl bromides and iodides under mild conditions.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1986, 1339-1340

Radical reactions in synthesis: carbon–carbon bond formation from 2-substituted allyl trialkyl stannanes

J. E. Baldwin, R. M. Adlington, D. J. Birch, J. A. Crawford and J. B. Sweeney, J. Chem. Soc., Chem. Commun., 1986, 1339 DOI: 10.1039/C39860001339

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