Issue 3, 1988

Mechanism of addition of silanediyls (silylenes) to buta-1,3-diene

Abstract

From experiments on the addition of :SiMeX (X = H, Cl, Me) to Buta-1,3-diene, it is concluded that the main cyclic adduct in each case results from initial 1,2-addition to form a vinylsilacyclopropane followed by a 1,3-silyl shift, rather than Si–C bond rupture.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1988, 241-243

Mechanism of addition of silanediyls (silylenes) to buta-1,3-diene

M. P. Clarke and I. M. T. Davidson, J. Chem. Soc., Chem. Commun., 1988, 241 DOI: 10.1039/C39880000241

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