Studies toward the Total Synthesis of Parvifolals A/B: An Intramolecular o-Quinone Methide [4 + 2]-Cycloaddition To Construct the Central Tetracyclic Core

[Image: see text] Two different approaches funded upon the intramolecular [4 + 2]-cycloaddition of in situ generated o-quinone methides have been explored to construct the central tetracyclic core of parvifolals A/B. At the outset, a cross-pinacol coupling of 2-formyl tri-O-methyl resveratrol with 4...

Descripción completa

Detalles Bibliográficos
Autores principales: Paymode, Dinesh J., Ramana, Chepuri V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2019
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6648467/
https://www.ncbi.nlm.nih.gov/pubmed/31459360
http://dx.doi.org/10.1021/acsomega.8b02777

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6648467/
https://www.ncbi.nlm.nih.gov/pubmed/31459360
http://dx.doi.org/10.1021/acsomega.8b02777

Ejemplares similares