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Enantioselective Total Synthesis of (−)-Acutumine

An account of the total synthesis of the tetracyclic alkaloid (−)-acutumine is presented. A first-generation approach to the spirocyclic subunit was unsuccessful due to incorrect regioselectivity in a radical cyclization. However, this work spawned a second-generation strategy in which the spirocycl...

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Detalhes bibliográficos
Main Authors: Li, Fang, Tartakoff, Samuel S., Castle, Steven L.
Formato: Artigo
Idioma:Inglês
Publicado em: 2009
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2790369/
https://ncbi.nlm.nih.gov/pubmed/19904909
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/jo902006q
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