Cargando…
A highly convergent synthesis of the C1–C31 polyol domain of amphidinol 3 featuring a TST-RCM reaction: confirmation of the revised relative stereochemistry
The concise enantioselective synthesis of the revised C1–C31 fragment of the polyketide amphidinol 3 was accomplished in 16 steps and 12.8% overall yield. Salient features of the strategy include chemoselective Weinreb amide coupling and concomitant CBS reduction for the preparation of the C1–C15 tr...
Autores principales: | Grisin, Aleksandr, Evans, P. Andrew |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5507186/ https://www.ncbi.nlm.nih.gov/pubmed/28757956 http://dx.doi.org/10.1039/c5sc00814j |
Ejemplares similares
-
Amphidinol 22, a New Cytotoxic and Antifungal Amphidinol from the Dinoflagellate Amphidinium carterae
por: Martínez, Kevin A., et al.
Publicado: (2019) -
Amphidinol 3 preferentially binds to cholesterol in disordered domains and disrupts membrane phase separation
por: Hieda, Manami, et al.
Publicado: (2021) -
TST (H=6) cycle
por: Evans, J
Publicado: (1989) -
TST (H = 6) cycle
por: Evans, J
Publicado: (1989) -
First Identification of Amphidinols from Mexican Strains and New Analogs
por: Durán-Riveroll, Lorena M., et al.
Publicado: (2023)