Cargando…
Quaternary stereocentres via catalytic enantioconvergent nucleophilic substitution reactions of tertiary alkyl halides by alkenylmetal reagents
The development of efficient methods, particularly catalytic and enantioselective processes, for the construction of all-carbon quaternary stereocentres is an important (and difficult) challenge in organic synthesis, due to the occurrence of this motif in a range of bioactive molecules. One conceptu...
Autores principales: | Wang, Zhaobin, Yang, Ze-Peng, Fu, Gregory C. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7925339/ https://www.ncbi.nlm.nih.gov/pubmed/33432109 http://dx.doi.org/10.1038/s41557-020-00609-7 |
Ejemplares similares
-
Stereospecific nucleophilic substitution at tertiary and quaternary stereocentres
por: Lanke, Veeranjaneyulu, et al.
Publicado: (2020) -
Formal enantioconvergent substitution of alkyl halides via catalytic asymmetric photoredox radical coupling
por: Li, Jiangtao, et al.
Publicado: (2018) -
A palladium-catalysed enolate alkylation cascade for the formation of adjacent quaternary and tertiary stereocentres
por: Streuff, Jan, et al.
Publicado: (2010) -
Catalytic Enantioconvergent Couplings of Secondary and Tertiary Electrophiles with Olefins
por: Wang, Zhaobin, et al.
Publicado: (2018) -
Quaternary Stereocenters via an Enantioconvergent Catalytic S(N)1 Reaction
por: Wendlandt, Alison E., et al.
Publicado: (2018)