Electrochemical Migratory Cyclization of N ‐Acylsulfonimide and N ‐Arylsulfonyl Benzothiamide
Year: 2026
Type: article
Abstract: An electrochemical migratory cyclization of N ‐acylsulfonylimine readily generates the biologically interesting sulfonylimine‐functionalized benzothiazine. The implementation of continuous flow electrolysis further enhances reaction efficiency and enables gram‐scale synthesis of this heterocyclic framework, providing the material basis for future biological activity studies. In addition, a straightforward electrochemical entry to the previously inaccessible benzothiazepine from N ‐arylsulfonyl benzothioamide is developed.
Source: Advanced Synthesis & Catalysis
DOI: 10.1002/adsc.70292
Institution: Fuzhou University
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: bronze
Award: G8607674867
OpenAlex ID: W7129087692
