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Total Synthesis of the Cyanolide A Aglycon
The synthesis of the potent molluscicide, cyanolide A, has been achieved in 10 steps without the use of protecting groups. The synthesis features a key Sakurai macrocyclization/dimerization reaction that simultaneously forms both tetrahydropyran rings and the macrocycle of the natural product.
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
2011
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3133735/ https://ncbi.nlm.nih.gov/pubmed/21639102 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/ja204228q |
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