An Unexpected Rearrangement of 2-(2-Benzofuranyl)-benzonitriles: a New Route to Phenylmethylene-dihydro-isoindolinones

DOI: 10.1039/c39880001604

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 1604 - 1605 (1988)

Update date:2022-08-02

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Authors:

Guillaumel, Jean

Boccara, Nicole

Demerseman, Pierre

Royer, Rene

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Article abstract of DOI:10.1039/c39880001604

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.

Full text of DOI:10.1039/c39880001604

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