Issue 24, 1988

An unexpected rearrangement of 2-(2-benzofuranyl)-benzonitriles: a new route to phenylmethylene-dihydro-isoindolinones

Abstract

Depending on the solvent used, the alkaline hydrolysis of 2-(2-benzofuranyl)-benzonitriles leads to the expected amide or acid, or to isoindolinones by rearrangement.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1988, 1604-1605

An unexpected rearrangement of 2-(2-benzofuranyl)-benzonitriles: a new route to phenylmethylene-dihydro-isoindolinones

J. Guillaumel, N. Boccara, P. Demerseman and R. Royer, J. Chem. Soc., Chem. Commun., 1988, 1604 DOI: 10.1039/C39880001604

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