Cargando…
Reductive Cross-Coupling of Olefins via a Radical Pathway
[Image: see text] Olefins are widely available at low costs, which explains the usefulness of developing new methods for their functionalization. Here we report a simple protocol that uses a photoredox catalyst and an inexpensive thiol catalyst to stitch together two olefins, forming a new C–C bond....
Autores principales: | Zhou, Wei, Dmitriev, Igor A., Melchiorre, Paolo |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10682986/ https://www.ncbi.nlm.nih.gov/pubmed/37947488 http://dx.doi.org/10.1021/jacs.3c11285 |
Ejemplares similares
-
Ruthenium(ii)-catalyzed olefination via carbonyl reductive cross-coupling
por: Wei, Wei, et al.
Publicado: (2017) -
Photo‐Organocatalytic Enantioselective Radical Cascade Reactions of Unactivated Olefins
por: Bonilla, Pablo, et al.
Publicado: (2018) -
Photochemical Organocatalytic
Functionalization of
Pyridines via Pyridinyl Radicals
por: Le Saux, Emilien, et al.
Publicado: (2022) -
A Practical
and Catalytic Reductive Olefin Coupling
por: Lo, Julian C., et al.
Publicado: (2014) -
Z-Selective Olefin Synthesis
via Iron-Catalyzed Reductive Coupling of Alkyl Halides with Terminal
Arylalkynes
por: Cheung, Chi Wai, et al.
Publicado: (2015)