Issue 9, 1976

Stereochemistry of bromofluorination of phenyl-substituted olefins

Abstract

Bromofluorination of phenyl-substituted olefins, e.g. 1,1-diphenylethylenes, β-alkylstyrenes, and stilbene, with N-bromosuccinimide–hydrogen fluoride–pyridine in ether proceeds with Markovnikov-type regioselectivity. The reaction is sterospecific (anti) for trans- and nonstereospecific for cis-olefins.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1976, 971-975

Stereochemistry of bromofluorination of phenyl-substituted olefins

M. Zupan and A. Pollak, J. Chem. Soc., Perkin Trans. 1, 1976, 971 DOI: 10.1039/P19760000971

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