Issue 15, 1988

An unusual ring closure reaction with formation of pyrrolidin-2,5-dione derivatives

Abstract

Mild oxidation of amidine (1) bearing two sterically crowded phenol moieties leads to the formation of the dispirocyclohexadienone derivative (6) of pyrrolidin-2,5-dione N-arylamine through an intramolecular ring closure recombination of the intermediate biradical (4).

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1988, 990-992

An unusual ring closure reaction with formation of pyrrolidin-2,5-dione derivatives

V. I. Minkin, E. P. Ivachnenko, A. I. Shif, L. P. Olekhnovitch, O. E. Kompan, A. I. Yanovskii and Y. T. Struchkov, J. Chem. Soc., Chem. Commun., 1988, 990 DOI: 10.1039/C39880000990

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