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Hydrosulfonylation of Alkenes with Sulfonyl Imines via Ir/Cu Dual Photoredox Catalysis.

Xian DuJing-Song ZhenXiao-Hong XuHan YuanYi-Hui LiYeqin ZhengCan XueYong Luo
Published in: Organic letters (2022)
Sulfonamides exhibit the advantages of wide prevalence, excellent prefunctionalization capability, and broad functional group compatibility. We report here utilizing sulfonyl imines as sulfonyl radical precursors for hydrosulfonylation of activated alkenes via visible-light irradiation. By preinstallation of functional groups into the sulfonamides and subsequent hydrosulfonylation, a variety of complex sulfones were synthesized with good efficiency under Ir/Cu dual photoredox catalysis. Additionally, this protocol expands the research in late-stage N-S bond modification in sulfonamides.
Keyphrases
  • visible light
  • solid phase extraction
  • randomized controlled trial
  • risk factors
  • aqueous solution
  • tandem mass spectrometry
  • electron transfer