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The Taumycin A Macrocycle: Asymmetric Total Synthesis and Revision of Relative Stereochemistry
[Image: see text] The first asymmetric total synthesis and revision of the relative configuration of the 12-membered taumycin A macrocycle is described. Key to the success of this work was a novel α-keto ketene macrocyclization that provided an efficient means by which to access two diastereomers of...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Chemical Society
2014
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4184443/ https://ncbi.nlm.nih.gov/pubmed/25248034 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/ol5025585 |
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