Cargando…
Quaternary Stereocenters via an Enantioconvergent Catalytic S(N)1 Reaction
The unimolecular nucleophilic substitution (S(N)1) mechanism figures prominently in every introductory organic chemistry course. In principle, stepwise displacement of a leaving group by a nucleophile via a carbocationic intermediate allows for the construction of highly congested carbon centers. Ho...
Autores principales: | Wendlandt, Alison E., Vangal, Prithvi, Jacobsen, Eric N. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6009832/ https://www.ncbi.nlm.nih.gov/pubmed/29695848 http://dx.doi.org/10.1038/s41586-018-0042-1 |
Ejemplares similares
-
Quaternary stereocentres via catalytic enantioconvergent nucleophilic substitution reactions of tertiary alkyl halides by alkenylmetal reagents
por: Wang, Zhaobin, et al.
Publicado: (2021) -
Catalytic enantioselective construction of vicinal quaternary carbon stereocenters
por: Zhou, Feng, et al.
Publicado: (2020) -
Stereospecific
Construction of Quaternary Carbon Stereocenters
from Quaternary Carbon Stereocenters
por: Patel, Kaushalendra, et al.
Publicado: (2022) -
Catalytic Enantioselective Entry to Triflones Featuring
a Quaternary Stereocenter
por: Franco, Francesca, et al.
Publicado: (2022) -
Enantioselective Construction of Remote Quaternary Stereocenters
por: Mei, Tian-Sheng, et al.
Publicado: (2014)