Enantioselective Synthesis of Fluorinated Indolizidinone Derivatives

[Image: see text] The enantioselective synthesis of fluorinated indolizidinone derivatives has been developed. The process involved an enantioselective intramolecular aza-Michael reaction of conjugated amides bearing a pendant α,β-unsaturated ketone moiety, catalyzed by the (S)-TRIP-derived phosphor...

Descripción completa

Detalles Bibliográficos
Autores principales: Escolano, Marcos, Gaviña, Daniel, Díaz-Oltra, Santiago, Sánchez-Roselló, María, del Pozo, Carlos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10186376/
https://www.ncbi.nlm.nih.gov/pubmed/37125898
http://dx.doi.org/10.1021/acs.orglett.3c00903

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10186376/
https://www.ncbi.nlm.nih.gov/pubmed/37125898
http://dx.doi.org/10.1021/acs.orglett.3c00903

Ejemplares similares