Cargando…
Enantioselective benzylic C–H arylation via photoredox and nickel dual catalysis
The asymmetric cross-coupling reaction is developed as a straightforward strategy toward 1,1-diaryl alkanes, which are a key skeleton in a series of natural products and bioactive molecules in recent years. Here we report an enantioselective benzylic C(sp(3))−H bond arylation via photoredox/nickel d...
Autores principales: | Cheng, Xiaokai, Lu, Huangzhe, Lu, Zhan |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6685991/ https://www.ncbi.nlm.nih.gov/pubmed/31391466 http://dx.doi.org/10.1038/s41467-019-11392-6 |
Ejemplares similares
-
Catalytic enantioselective reductive domino alkyl arylation of acrylates via nickel/photoredox catalysis
por: Qian, Pengcheng, et al.
Publicado: (2021) -
Asymmetric benzylic C(sp(3))−H acylation via dual nickel and photoredox catalysis
por: Huan, Leitao, et al.
Publicado: (2021) -
C–H functionalization of amines with aryl halides by nickel-photoredox catalysis
por: Ahneman, Derek T., et al.
Publicado: (2016) -
Asymmetric β-arylation of cyclopropanols enabled by photoredox and nickel dual catalysis
por: Wang, Jianhua, et al.
Publicado: (2022) -
Direct α-Arylation/Heteroarylation of
2-Trifluoroboratochromanones via Photoredox/Nickel
Dual Catalysis
por: Matsui, Jennifer K., et al.
Publicado: (2017)