Cargando…
Benzylic C(sp(3))–C(sp(2)) cross-coupling of indoles enabled by oxidative radical generation and nickel catalysis
A mechanistically unique functionalization strategy for a benzylic C(sp(3))–H bond has been developed based on the facile oxidation event of indole substrates. This novel pathway was initiated by efficient radical generation at the benzylic position of the substrate, with subsequent transition metal...
Autores principales: | Kim, Weonjeong, Koo, Jangwoo, Lee, Hong Geun |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8179435/ https://www.ncbi.nlm.nih.gov/pubmed/34163683 http://dx.doi.org/10.1039/d0sc06666d |
Ejemplares similares
-
Nickel catalysis enables convergent paired electrolysis for direct arylation of benzylic C–H bonds
por: Zhang, Lei, et al.
Publicado: (2020) -
Asymmetric benzylic C(sp(3))−H acylation via dual nickel and photoredox catalysis
por: Huan, Leitao, et al.
Publicado: (2021) -
Site-selective coupling of remote C(sp(3))–H/meta-C(sp(2))–H bonds enabled by Ru/photoredox dual catalysis and mechanistic studies
por: Liu, Hong-Chao, et al.
Publicado: (2022) -
Reductive coupling of benzyl oxalates with highly functionalized alkyl bromides by nickel catalysis
por: Yan, Xiao-Biao, et al.
Publicado: (2018) -
Transition-metal-free C(sp(3))–H/C(sp(3))–H dehydrogenative coupling of saturated heterocycles with N-benzyl imines
por: Liu, Zhengfen, et al.
Publicado: (2020)