THE REARRANGEMENT OF ARYLSELENENAMIDES |
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| Authors: | P T Southwell-keely I L Johnstone E R Cole |
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| Institution: | 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 |
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| Abstract: | 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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