A palladium-catalyzed three-component tandem reaction of thioamides, arenediazonium tetrafluoroborates and DABSO: an efficient synthesis of arylsulfonyl 1,3-benzothiazines
Abstract
insertion/cyclization process. The transformation proceeds under mild conditions with broad substrate scope, accommodating various aryl, heteroaryl, and alkyl-substituted thioamides as well as diverse diazonium salts, providing the corresponding sulfonylated benzothiazines in moderate to good yields.
Fields of Study & Subjects
Sulfur-Based Synthesis Techniques
Catalytic C–H Functionalization Methods
Synthesis and Reactivity of Sulfur-Containing Compounds
Publication details
- Journal / source
- Chemical Communications
- Publisher
- Royal Society of Chemistry (RSC)
- Volume
- 62
- Issue
- 47
- Pages
- 11936–11939
- Publication date
- 1 January 2026
- Language
- EN