Issue 2, 1994

A mechanistic study of quinoxaline formation

Abstract

Benzil 2 reacts readily with 1,2-phenylenediamine 1 to give 2,3-diphenylquinoxaline 3. By the use of 13C NMR spectroscopy with a labelled substrate the course of the reaction has been determined. A parallel study of the reaction between benzil and 6-methoxy-2,4,5-triaminopyrimidine gave only an indication of the pathway because of the large number of possible intermediates.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1994, 323-326

A mechanistic study of quinoxaline formation

L. M. Anderson and A. R. Butler, J. Chem. Soc., Perkin Trans. 2, 1994, 323 DOI: 10.1039/P29940000323

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