Cargando…
Oxidative organocatalysed enantioselective coupling of indoles with aldehydes that forms quaternary carbon stereocentres
The first organocatalysed, metal-free cross-nucleophile coupling of indoles with α-branched aldehydes forming acyclic stereoselective quaternary carbon centres is presented. Applying an amino acid-derived catalyst with suitable organic oxidants affords the desired enantioenriched indole functionalis...
Autores principales: | Rezayee, Nomaan M., Lauridsen, Vibeke H., Næsborg, Line, Nguyen, Thanh V. Q., Tobiesen, Henriette N., Jørgensen, Karl Anker |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6432613/ https://www.ncbi.nlm.nih.gov/pubmed/30996950 http://dx.doi.org/10.1039/c9sc00196d |
Ejemplares similares
-
Enantioselective allylic alkylation of stereodefined polysubstituted copper enolates as an entry to acyclic quaternary carbon stereocentres
por: Nairoukh, Zackaria, et al.
Publicado: (2017) -
Stereospecific nucleophilic substitution at tertiary and quaternary stereocentres
por: Lanke, Veeranjaneyulu, et al.
Publicado: (2020) -
Atroposelective brominations to access chiral biaryl scaffolds using high-valent Pd-catalysis
por: Linde, Sif T., et al.
Publicado: (2023) -
Parts-per-million level loading organocatalysed enantioselective silylation of alcohols
por: Park, Sang Yeon, et al.
Publicado: (2015) -
A palladium-catalysed enolate alkylation cascade for the formation of adjacent quaternary and tertiary stereocentres
por: Streuff, Jan, et al.
Publicado: (2010)