Cargando…
A C–H bond activation-based catalytic approach to tetrasubstituted chiral allenes
Enantioselective synthesis of fully substituted allenes has been a challenge due to the non-rigid nature of the axial chirality, which spreads over three carbon atoms. Here we show the commercially available simple Rh complex may catalyse the CMD (concerted metalation/deprotonation)-based reaction o...
Autores principales: | Wu, Shangze, Huang, Xin, Wu, Wangteng, Li, Pengbin, Fu, Chunling, Ma, Shengming |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4918348/ https://www.ncbi.nlm.nih.gov/pubmed/26246391 http://dx.doi.org/10.1038/ncomms8946 |
Ejemplares similares
-
Palladium-catalysed formation of vicinal all-carbon quaternary centres via propargylation
por: Huang, Xin, et al.
Publicado: (2016) -
Catalytic enantioselective construction of axial chirality in 1,3-disubstituted allenes
por: Song, Shihua, et al.
Publicado: (2019) -
Organocatalytic synthesis of chiral tetrasubstituted allenes from racemic propargylic alcohols
por: Qian, Deyun, et al.
Publicado: (2017) -
Copper-catalyzed propargylic C–H functionalization for allene syntheses
por: Zhang, Dongjie, et al.
Publicado: (2023) -
Rhodium-catalyzed C–H functionalization-based approach to eight-membered lactams
por: Wu, Shangze, et al.
Publicado: (2015)