Issue 0, 1971

Aspects of tautomerism. Part II. Reactions of the pseudo-acid chloride of o-benzoylbenzoic acid with nucleophiles

Abstract

Reactions of fourteen nucleophiles with the pseudo-acid chloride of o-benzoylbenzoic acid in two solvents have been studied. The nucleophiles that react primarily at the tetrahedral carbon atom to give pseudo derivatives, are weaker than those that react at the carbonyl carbon atom causing opening of the lactone ring. An explanation for this phenomenon is advanced.

Article information

Article type
Paper

J. Chem. Soc. C, 1971, 1772-1777

Aspects of tautomerism. Part II. Reactions of the pseudo-acid chloride of o-benzoylbenzoic acid with nucleophiles

M. V. Bhatt, K. M. Kamath and M. Ravindranathan, J. Chem. Soc. C, 1971, 1772 DOI: 10.1039/J39710001772

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