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A Concise Asymmetric Total Synthesis of (+)-Brevisamide
[Image: see text] A new protecting-group-free synthesis of the marine monocyclic ether (+)-brevisamide is reported. The enantioselective synthesis utilizes a key asymmetric Henry reaction and an Achmatowicz rearrangement for the formation of the tetrahydropyran ring. A penultimate Stille cross-coupl...
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| Autors principals: | , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2011
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3365585/ https://ncbi.nlm.nih.gov/pubmed/21678904 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/ol201283n |
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