Issue 17, 1988

Rearrangement reactions in 1-methyl-2-vinylsilacyclopropane

Abstract

1-Methyl-2-vinylsilacyclopropane, formed by addition of methylsilanediyl (methylsilylene) to buta-1,3-diene, is shown by deuterium labelling to undergo rearrangements initiated by both a 1,2- and a 1,5-hydrogen shift; the former is more important, especially at lower temperature.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1988, 1139-1141

Rearrangement reactions in 1-methyl-2-vinylsilacyclopropane

M. P. Clarke, I. M. T. Davidson and M. P. Dillon, J. Chem. Soc., Chem. Commun., 1988, 1139 DOI: 10.1039/C39880001139

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