Issue 0, 1971

Aspects of tautomerism. Part III. A new dimerisation reaction of pseudo-acid chlorides

Abstract

Pseudo-acid chlorides of five 4′-substituted o-benzoylbenzoic acids are converted into a mixture of dilactones with sodium iodide in acetone. The meso-isomer is always formed to a larger extent than the (±)-mixture. These results imply that the radicals involved are not planar.

Article information

Article type
Paper

J. Chem. Soc. C, 1971, 3344-3347

Aspects of tautomerism. Part III. A new dimerisation reaction of pseudo-acid chlorides

M. V. Bhatt, K. M. Kamath and M. Ravindranathan, J. Chem. Soc. C, 1971, 3344 DOI: 10.1039/J39710003344

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