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REDUCTIVE DEIMINATION OF SULFOXIMIDES AND SULFIMIDES WITH P-TOLUENESULFONYL NITRITE AND T-BUTYL THIONITRATE1
Authors:Shigeru Oae  Kazuyuki Iida  Toshikazu Takata
Institution:Department of Chemistry , The University of Tsukuba , Sakura, Ibaraki, 305, Japan
Abstract:Abstract

Reduction of sulfimides and sulfoximides with p-toluenesulfonyl nitrite, a new nitrosating agent, gave nearly quantitatively the corresponding deimination products, sulfides and sulfoxides, respectively. In the reaction of dialkyl and aryl alkyl sulfoximides with t-butyl thionitrate, N-t-butylthiosulfoximides were obtained besides the usual deimination products, although diaryl sulfoximides were readily deiminated to the corresponding sulfoxides in good yields in the same treatment. t-Butyl thionitrate was also found to deiminate diphenyl sulfimide to give diphenyl sulfide in good yield. Sulfoximides reacted sluggishly with t-butyl thionitrite, however, eventually affording a small amount of sulfoxides.
Keywords:N-(2-cyano-1-methyl-etheny1)-O  O-diphenyl-amido-phosphate  N-(2-cyano-1-methyl-ethenyl)-O  O-diphenyl-amido-thiophosphate  N-(diphenoxy-thiophosphoryl)-3-amino-crotonitrile  N-(O  O-diphenyl-thiophosphatyl)-3-amino-crotonitrile  acetonitrile  diphenoxyphosphorylchloride  diphenoxythiophosphorylchloride  x-ray structure analysis  hydrogen bonds
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