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Rapid Access to Conformational Analogues of (+)-Peloruside A

[Image: see text] An efficient synthetic strategy for rapid access to analogues of peloruside A has been demonstrated. The synthetic route was highlighted by a simple esterification-based fragment coupling and a late stage ring-closing metathesis reaction. This convergent route has provided access t...

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Detalhes bibliográficos
Main Authors: Zhao, Zhiming, Taylor, Richard E.
Formato: Artigo
Idioma:Inglês
Publicado em: 2012
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3272296/
https://ncbi.nlm.nih.gov/pubmed/22235754
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/ol203268t
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