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