Cu-catalyzed N–S bond coupling between hydroxylamines and sulfinic acids: rapid access to N -arylsulfonamides
Abstract
-arylsulfonamides without additional oxidants has been demonstrated. The protocol features the advantages of operational simplicity, environmental friendliness and mild reaction conditions. Mechanistic studies have shown that hydroxylamine exhibits unique multifunctionality in this reaction, serving as a reducing reagent, an amine donor, and a potential oxidant.
Fields of Study & Subjects
Sulfur-Based Synthesis Techniques
Catalytic C–H Functionalization Methods
Catalytic Cross-Coupling Reactions
Publication details
- Journal / source
- Organic & Biomolecular Chemistry
- Publisher
- Royal Society of Chemistry (RSC)
- Volume
- 24
- Issue
- 5
- Pages
- 1021–1026
- Publication date
- 1 January 2026
- Language
- EN