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Enantioselective Formal Synthesis of (−)-Englerin A via a Rh-catalyzed [4+3] Cycloaddition Reaction

[Image: see text] An enantioselective formal synthesis of (−)-englerin A (1) is reported. Key to the strategy is a Rh-catalyzed [4+3] cycloaddition reaction between furan 10 and diazoester 11 that, following an intramolecular aldol condensation, produces the tri-cyclic scaffold of englerin. This str...

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Detalhes bibliográficos
Main Authors: Xu, Jing, Caro-Diaz, Eduardo J.E., Theodorakis, Emmanuel A.
Formato: Artigo
Idioma:Inglês
Publicado em: 2010
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2927118/
https://ncbi.nlm.nih.gov/pubmed/20669919
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/ol1015652
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