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Toward the total synthesis of maoecrystal V: an intramolecular Diels–Alder route to the maoecrystal V pentacyclic core with the appropriate relative stereochemistry

A diastereoselective route to the maoecrystal V core compound (6) has been achieved. Key transformations include an intramolecular Diels–Alder cyclization and an exo-glycal epoxide rearrangement sequence.

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Detalhes bibliográficos
Main Authors: Peng, Feng, Danishefsky, Samuel J.
Formato: Artigo
Idioma:Inglês
Publicado em: 2011
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3079889/
https://ncbi.nlm.nih.gov/pubmed/21516211
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.tetlet.2010.11.029
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