THE REARRANGEMENT OF ARYLSELENENAMIDES

P. T. Southwell-keely School of Wool and Pastoral Sciences and the Department of Applied Organic Chemistry, The University of New South Wales, Kensington, N.S. W., 2033, Australia

I. L. Johnstone School of Wool and Pastoral Sciences and the Department of Applied Organic Chemistry, The University of New South Wales, Kensington, N.S. W., 2033, Australia

E. R. Cole School of Wool and Pastoral Sciences and the Department of Applied Organic Chemistry, The University of New South Wales, Kensington, N.S. W., 2033, Australia

Abstract

Attempts to synthesize N-phenylbenzeneselenena mide always produced the isomeric p-aminodiphenyl selenide, probably as a result of an acid catalyzed rearrangement. The ease with which this rearrangement occurs is contrasted with the forcing conditions required for the analogous rearrangement of sulfenamides.

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THE REARRANGEMENT OF ARYLSELENENAMIDES

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THE REARRANGEMENT OF ARYLSELENENAMIDES

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