Cargando…
Investigations into mechanism and origin of regioselectivity in the metallaphotoredox-catalyzed α-arylation of N-alkylbenzamides
A mechanistic study on the α-arylation of N-alkylbenzamides catalyzed by a dual nickel/photoredox system using aryl bromides is reported herein. This study elucidates the origins of site-selectivity of the transformation, which is controlled by the generation of a hydrogen atom transfer (HAT) agent...
Autores principales: | Rand, Alexander W., Chen, Mo, Montgomery, John |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9473500/ https://www.ncbi.nlm.nih.gov/pubmed/36277638 http://dx.doi.org/10.1039/d2sc01962k |
Ejemplares similares
-
Metallaphotoredox Aryl and Alkyl Radiomethylation for PET Ligand Discovery
por: Pipal, Robert W., et al.
Publicado: (2020) -
Palladium-Catalyzed Regioselective Arylation of Unprotected
Allylamines
por: Landge, Vinod G., et al.
Publicado: (2020) -
Catalytic reduction of aryl trialkylammonium salts to aryl silanes and arenes
por: Rand, Alexander W., et al.
Publicado: (2019) -
Regioselective Pd-catalyzed α-alkylation of furans using alkyl iodides
por: Yuan, Jiaqi, et al.
Publicado: (2021) -
Nickel-catalyzed asymmetric reductive arylation of α-chlorosulfones with aryl halides
por: Sun, Deli, et al.
Publicado: (2021)