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Synthesis of Aromatic Sulfonamides through a Copper-Catalyzed Coupling of Aryldiazonium Tetrafluoroborates, DABCO·(SO2)2, and N-Chloroamines.

Feng ZhangDanqing ZhengLifang LaiJiang ChengJiangtao SunJie Wu
Published in: Organic letters (2018)
A copper-catalyzed aminosulfonylation of aryldiazonium tetrafluoroborates, DABCO·(SO2)2, and N-chloroamines is described. This coupling reaction provides an efficient and simple approach to a wide range of sulfonamides in moderate to good yields under mild conditions. Mechanistic investigation suggests that a radical process and transition-metal catalysis are merged in this tandem reaction.
Keyphrases
  • transition metal
  • electron transfer
  • room temperature
  • solid phase extraction
  • high intensity
  • amino acid
  • high resolution
  • simultaneous determination