Cargando…
1,4-Dihydropyridines as Alkyl Radical Precursors: Introducing the Aldehyde Feedstock to Nickel/Photoredox Dual Catalysis
[Image: see text] A Ni/photoredox dual catalytic cross-coupling is disclosed in which a diverse range of (hetero)aryl bromides are used as electrophiles, with 1,4-dihydropyridines serving as precursors to C(sp)(3)-centered alkyl radical coupling partners. The reported method is characterized by its...
Autores principales: | Gutiérrez-Bonet, Álvaro, Tellis, John C., Matsui, Jennifer K., Vara, Brandon A., Molander, Gary A. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2016
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5152669/ https://www.ncbi.nlm.nih.gov/pubmed/27990318 http://dx.doi.org/10.1021/acscatal.6b02786 |
Ejemplares similares
-
Thioetherification via Photoredox/Nickel Dual Catalysis
por: Jouffroy, Matthieu, et al.
Publicado: (2016) -
Olefination of Alkyl Halides with Aldehydes by Merging Visible-Light Photoredox Catalysis and Organophosphorus Chemistry
por: Jiang, Min, et al.
Publicado: (2018) -
Single-Electron Transmetalation: Protecting-Group-Independent
Synthesis of Secondary Benzylic Alcohol Derivatives via Photoredox/Nickel
Dual Catalysis
por: Karimi-Nami, Rahman, et al.
Publicado: (2016) -
Direct α-Arylation/Heteroarylation of
2-Trifluoroboratochromanones via Photoredox/Nickel
Dual Catalysis
por: Matsui, Jennifer K., et al.
Publicado: (2017) -
Formal β‐C−H Arylation of Aldehydes and Ketones by Cooperative Nickel and Photoredox Catalysis
por: Liu, Kun, et al.
Publicado: (2022)