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An efficient and mild oxidative approach from thiols to sulfonyl derivatives with DMSO/HBr.

Hongye WangZhaoting LiRongheng DaiNing JiaoSong Song
Published in: Chemical science (2023)
A mild and practical method for synthesizing sulfonyl derivatives, which have a wide range of applications in pharmaceuticals, materials, and organic synthesis, was described through the oxidative functionalization of thiols with DMSO/HBr. The simple conditions, low cost and ready availability of DMSO/HBr, as well as the versatility of the transformations, make this strategy very powerful in synthesizing a variety of sulfonyl derivatives including sulfonamides, sulfonyl fluorides, sulfonyl azides, and sulfonates. Mechanistic studies revealed that DMSO served as the terminal oxidant, and HBr acted as both a nucleophile and a redox mediator to transfer the oxygen atom.
Keyphrases
  • low cost
  • structure activity relationship
  • molecular dynamics
  • single cell
  • electron transfer
  • high resolution
  • liquid chromatography