Reductive elimination in vicinal dibromides. Electrochemical reduction of 1,2-dibromo-3-(4-substituted)-phenylpropanes and induction of double-bond migration in the resulting olefins.

doi:10.1016/S0022-0728(94)87014-4

Paper

DOI: 10.1016/S0022-0728(94)87014-4

Reductive elimination in vicinal dibromides. Electrochemical reduction of 1,2-dibromo-3-(4-substituted)-phenylpropanes and induction of double-bond migration in the resulting olefins.

Published Jun 27, 1994 · C. Andrieux, Annie Le Gorande, J. Savéant

Journal of Electroanalytical Chemistry

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Abstract

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Study Snapshot

Electrochemical reduction of 1,2-dibromo-3(4-substituted)-phenylpropanes leads to reductive cleavage of the 2-carbon-bromine bond, resulting in the stable 1,2-olefin and double-bond migration.

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

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