Photoredox-Catalyzed Giese Reactions: Decarboxylative Additions to Cyclic Vinylogous Amides and Esters

An effective strategy has been developed for the photoredox-catalyzed decarboxylative addition of cyclic amino acids to both vinylogous amides and esters leading to uniquely substituted heterocycles. The additions take place exclusively trans to the substituent present on the dihydropyridone ring af...

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Detalles Bibliográficos
Autores principales: Dykstra, Kevin, Buevich, Alexei, Gao, Qi, Lam, Yu-Hong, Kuethe, Jeffrey T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8777773/
https://www.ncbi.nlm.nih.gov/pubmed/35056732
http://dx.doi.org/10.3390/molecules27020417

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8777773/
https://www.ncbi.nlm.nih.gov/pubmed/35056732
http://dx.doi.org/10.3390/molecules27020417

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