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Enantioselective Synthesis of the 5-6-7 Carbocyclic Core of the Gagunin Diterpenoids

[Image: see text] A catalytic enantioselective double allylic alkylation reaction has been employed in the synthesis of the core of the gagunin diterpenoids. Enantioenriched material was advanced in eleven steps to afford the core of the highly-oxygenated target, which includes two all-carbon quater...

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Bibliografiska uppgifter
Huvudupphovsmän: Shibuya, Grant M., Enquist, John A., Stoltz, Brian M.
Materialtyp: Artigo
Språk:Inglês
Publicerad: 2013
Ämnen:
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC3743267/
https://ncbi.nlm.nih.gov/pubmed/23802176
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/ol401514s
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