| Literature DB >> 11429835 |
A L Marzinzik1, K B Sharpless.
Abstract
While excellent methods exist for the oxidation of sulfides to sulfoxides R1R2S-->R1R2SO, the azaversion of this atom transfer redox process, i.e., R1R2S-->R1R2S=N-SO2R3, has been less reliable. In sulfilimine synthesis, sulfoxide has been an inevitable byproduct in all cases to date, and the yields of sulfilimine have varied widely. A nearly ideal procedure for the sulfide to sulfonyl sulfilimine transformation is described. Almost quantitative yields are achieved from a diverse set of sulfides and a broad range of the readily available sulfonyl nitrenoid sources known as chloramine salts (R3SO2NClNa), essentially by simply stirring them together in acetonitrile.Entities:
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Year: 2001 PMID: 11429835 DOI: 10.1021/jo0012039
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354