Issue 22, 1970

Novel rearrangements occurring during the thermolysis of 2,3-diphenyl-2H-azirine

Abstract

G.l.c. treatment of 2,3-diphenyl-2H-azirine at 220° yields 2-phenylindole: heating 2,3-diphenyl-2H-azirine at 250° in a sealed tube produces 2-phenylindole, 2,4,5-triphenylimidazole, 1-benzyl-2,4,5-triphenylimidazole, and 2,3,4,5-tetraphenylpyrrole as major products.

Article information

Article type
Paper

J. Chem. Soc. D, 1970, 1565-1566

Novel rearrangements occurring during the thermolysis of 2,3-diphenyl-2H-azirine

J. H. Bowie and B. Nussey, J. Chem. Soc. D, 1970, 1565 DOI: 10.1039/C29700001565

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