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(+)-Sorangicin A: evolution of a viable synthetic strategy
An effective, asymmetric total synthesis of the antibiotic (+)-sorangicin A (1) has been achieved. Central to this venture was the development of first and second generation syntheses of the signature dioxabicyclo[3.2.1]octane core, the first featuring chemo- and stereoselective epoxide ring opening...
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Main Authors: | , , , , , |
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Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
2011
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Assuntos: | |
Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3254116/ https://ncbi.nlm.nih.gov/pubmed/22247573 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.tet.2011.09.035 |
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