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Enantioselective Synthesis of (+)-Hippolide J and Reevaluation of Antifungal Activity
A synthesis of the reported antifungal agent (+)-hippolide J is presented. The rapid assembly of the natural product was enabled through implementation of an enantioselective isomerization/[2 + 2]-cycloaddition sequence. Due to the simplicity of the route, >100 mg of the natural product were prep...
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| Publicado en: | Org Lett |
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| Autores principales: | , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
2020
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7824975/ https://ncbi.nlm.nih.gov/pubmed/32969231 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/acs.orglett.0c02979 |
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