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Thioesters as Bifunctional Reagents for 2‐Naphthylamine Sulfuracylation.
- Source :
-
Advanced Synthesis & Catalysis . 7/11/2019, Vol. 361 Issue 14, p3331-3336. 6p. - Publication Year :
- 2019
-
Abstract
- An efficient and convenient strategy for the preparation of diaryl sulfides via a Fe‐promoted direct sulfuracylation of 2‐naphthylamine using thioesters as bifunctional reagents is described. This synthetic strategy features high chemoselectivity, good substrate scope and functional group tolerance. [ABSTRACT FROM AUTHOR]
- Subjects :
- *THIOESTERS
*FUNCTIONAL groups
*CHEMOSELECTIVITY
*SULFIDES
Subjects
Details
- Language :
- English
- ISSN :
- 16154150
- Volume :
- 361
- Issue :
- 14
- Database :
- Academic Search Index
- Journal :
- Advanced Synthesis & Catalysis
- Publication Type :
- Academic Journal
- Accession number :
- 137489640
- Full Text :
- https://doi.org/10.1002/adsc.201900301