This is the authors' abstract. We don't add key points for this paper.
A copper-catalyzed aminosulfonylation of aryldiazonium tetrafluoroborates, DABCO·(SO 2 ) 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.
Answers are grounded in this paper and cite their sources.
No takes yet. Share an insight, caveat, or question.
Zhang et al. (2018) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: