Issue 1, 1982

Studies in decarboxylation. Part 15. The effect of 3-substitution on the rate of decarboxylation of βγ-unsaturated acids

Abstract

The kinetic effect of substituents at C(3) of βγ-unsaturated acids is consistent with the development of a partial positive charge at that position during decarboxylation. The OMe group increases the rate of decarboxylation as much as 105–106 fold.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1982, 15-17

Studies in decarboxylation. Part 15. The effect of 3-substitution on the rate of decarboxylation of βγ-unsaturated acids

A. Al-Borno and D. B. Bigley, J. Chem. Soc., Perkin Trans. 2, 1982, 15 DOI: 10.1039/P29820000015

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