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Stereoselective Synthesis of the I–L Fragment of the Pacific Ciguatoxins
The I–L ring system found in all the Pacific ciguatoxins has been prepared from a tricyclic precursor in a highly stereoselective manner. Subtle differences in the reactivity of the enones present in the seven- and eight-membered rings of the tricyclic ether starting material have been exploited to...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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MDPI
2020
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7760828/ https://www.ncbi.nlm.nih.gov/pubmed/33255410 http://dx.doi.org/10.3390/toxins12120740 |