Enantioselective palladaelectro-catalyzed C–H olefinations and allylations for N–C axial chirality

Enantioselective palladaelectro-catalyzed C–H alkenylations and allylations were achieved with easily-accessible amino acids as transient directing groups. This strategy provided access to highly enantiomerically-enriched N–C axially chiral scaffolds under exceedingly mild conditions. The synthetic...

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Detalles Bibliográficos
Autores principales: Dhawa, Uttam, Wdowik, Tomasz, Hou, Xiaoyan, Yuan, Binbin, Oliveira, João C. A., Ackermann, Lutz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Chemistry
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8565398/
https://www.ncbi.nlm.nih.gov/pubmed/34760203
http://dx.doi.org/10.1039/d1sc04687j

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8565398/
https://www.ncbi.nlm.nih.gov/pubmed/34760203
http://dx.doi.org/10.1039/d1sc04687j

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