Enantioselective total synthesis of parnafungin A1 and 10a-epi-hirtusneanine

The first and enantioselective total synthesis of the heterodimeric biaryl antifungal natural product parnafungin A1 as well as complex biaryl tetrahydroxanthone 10a-epi-hirtusneanine is accomplished, by employing cross-coupling through the benzoxaborole strategy to construct their sterically hinder...

Descripción completa

Detalles Bibliográficos
Autores principales: Sun, Jiawei, Gu, Wei, Yang, He, Tang, Wenjun
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/PMC8336460/
https://www.ncbi.nlm.nih.gov/pubmed/34377417
http://dx.doi.org/10.1039/d1sc02919c

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8336460/
https://www.ncbi.nlm.nih.gov/pubmed/34377417
http://dx.doi.org/10.1039/d1sc02919c

Ejemplares similares