N,N,N',N'-Tetramethylethylenediamine-Enabled Photoredox-Catalyzed C-H Methylation of N-Heteroarenes.
J Org Chem
; 86(17): 11905-11914, 2021 09 03.
Article
en En
| MEDLINE
| ID: mdl-34344150
Aiming at the valuable methylation process, readily available and inexpensive N,N,N',N'-tetramethylethylenediamine (TMEDA) was first identified as a new methyl source in photoredox-catalyzed transformation in this work. By virtue of this simple methylating reagent, a facile and practical protocol for the direct C-H methylation of N-heteroarenes was developed, featuring mild reaction conditions, broad substrate scope, and scalability. Mechanistic studies disclosed that a sequential photoredox, base-assisted proton shift, fragmentation, and tautomerization process was essentially involved.
Texto completo:
1
Colección:
01-internacional
Base de datos:
MEDLINE
Asunto principal:
Protones
/
Etilenodiaminas
Tipo de estudio:
Guideline
Idioma:
En
Revista:
J Org Chem
Año:
2021
Tipo del documento:
Article
Pais de publicación:
Estados Unidos