Cargando…
Investigating the Mechanism of Ni-Catalyzed Coupling of Photoredox-Generated Alkyl Radicals and Aryl Bromides: A Computational Study
Photoredox catalysis has emerged as an alternative to classical cross-coupling reactions, promoting new reactivities. Recently, the use of widely abundant alcohols and aryl bromides as coupling reagents was demonstrated to promote efficient coupling through the Ir/Ni dual photoredox catalytic cycle....
Autores principales: | Sanosa, Nil, Ruiz-Campos, Pedro, Ambrosi, Diego, Sampedro, Diego, Funes-Ardoiz, Ignacio |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10252489/ https://www.ncbi.nlm.nih.gov/pubmed/37298098 http://dx.doi.org/10.3390/ijms24119145 |
Ejemplares similares
-
Mechanism of the Aza-Piancatelli Reaction: Scope and
Limitations of Furan Substitution in Donor–Acceptor Stenhouse
Adduct Synthesis
por: Peñín, Beatriz, et al.
Publicado: (2022) -
Mild and Chemoselective Carboxylic Acid Reduction Promoted by Borane Catalysis
por: Lunic, Danijela, et al.
Publicado: (2022) -
Amide Synthesis by Nickel/Photoredox‐Catalyzed Direct Carbamoylation of (Hetero)Aryl Bromides
por: Alandini, Nurtalya, et al.
Publicado: (2020) -
Silyl-mediated photoredox-catalyzed Giese reaction: addition of non-activated alkyl bromides
por: ElMarrouni, Abdellatif, et al.
Publicado: (2018) -
Nickel-catalysed cross-electrophile coupling of aryl bromides and primary alkyl bromides
por: Gao, Nanxing, et al.
Publicado: (2022)