Issue 2, 1976

Mechanisms of addition. Part II. The stereochemistry of addition of bromine and bromine acetate to some phenyl-substituted olefins

Abstract

The addition of bromine acetate to some phenyl-substituted olefins is, more stereospecific than the corresponding additions of chlorine acetate. The stereochemistry of addition of bromine to methyl para-methyl-trans-cinnamate depends on concentration. The results have mechanistic implications.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1976, 141-147

Mechanisms of addition. Part II. The stereochemistry of addition of bromine and bromine acetate to some phenyl-substituted olefins

M. A. Wilson and P. D. Woodgate, J. Chem. Soc., Perkin Trans. 2, 1976, 141 DOI: 10.1039/P29760000141

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