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Enantioselective Syntheses of Wickerols A and B

[Image: see text] The evolution of a successful strategy for the synthesis of the strained, cage-like antiviral diterpenoids wickerols A and B is described. Initial attempts to access the carbocyclic core were surprisingly challenging and in retrospect, presaged the many detours needed to ultimately...

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Detalles Bibliográficos
Autores principales: Chung, Jonathan, Capani, Joseph S., Göhl, Matthias, Roosen, Philipp C., Vanderwal, Christopher D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10037325/
https://www.ncbi.nlm.nih.gov/pubmed/36883956
http://dx.doi.org/10.1021/jacs.3c00448