Back to Search
Start Over
Electrosynthesis of Thiocyanated/Iodinated/Brominated Pyrazol‐5‐amines and Thiocyanated Enamines via C(sp2)−H Functionalization.
- Source :
-
Advanced Synthesis & Catalysis . 6/13/2023, Vol. 365 Issue 11, p1782-1787. 6p. - Publication Year :
- 2023
-
Abstract
- An electrochemical method for the C(sp2)−H thiocyanation of pyrazol‐5‐amines and enamines were developed in an undivided cell. A variety of thiocyanated pyrazol‐5‐amine and enamine derivatives were accessed in 36–91% yields, employing thiocyanate salts as electrolyte and thiocyanating reagent. Moreover, this electrochemical protocol can be extended to the synthesis of various iodinated and brominated pyrazol‐5‐amine derivatives in 51–95% yields. This electrochemical protocol does not require a metal or external chemical oxidants and tolerates unprotected amino groups. [ABSTRACT FROM AUTHOR]
- Subjects :
- *ENAMINES
*AMINO group
*ELECTROSYNTHESIS
*OXIDIZING agents
Subjects
Details
- Language :
- English
- ISSN :
- 16154150
- Volume :
- 365
- Issue :
- 11
- Database :
- Academic Search Index
- Journal :
- Advanced Synthesis & Catalysis
- Publication Type :
- Academic Journal
- Accession number :
- 164284758
- Full Text :
- https://doi.org/10.1002/adsc.202300255