Desymmetrization of pibrentasvir for efficient prodrug synthesis

A novel and practical desymmetrization tactic is described to access a new class of pibrentasvir prodrugs. The homotopic benzimidazoles of pibrentasvir (PIB) are differentiated via a one-pot di-Boc/mono-de-Boc selective N-Boc protection and formaldehyde adduct formation sequence, both enabled by cry...

Descripción completa

Detalles Bibliográficos
Autores principales: Voight, Eric A., Greszler, Stephen N., Hartung, John, Ji, Jianguo, Klix, Russell C., Randolph, John T., Shelat, Bhadra H., Waters, Jan E., DeGoey, David A.
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/PMC8317637/
https://www.ncbi.nlm.nih.gov/pubmed/34349971
http://dx.doi.org/10.1039/d1sc02396a

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8317637/
https://www.ncbi.nlm.nih.gov/pubmed/34349971
http://dx.doi.org/10.1039/d1sc02396a

Ejemplares similares