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Concise, Biomimetic Total Synthesis of d,l-Marcfortine C
A biomimetic total synthesis of the fungal metabolite marcfortine C utilizing an intramolecular Diels-Alder reaction is described. In addition, a key stereoselective oxaziridine-mediated oxidation/pinacol rearrangement of indole 24 was used to complete the total synthesis.
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| Glavni autori: | , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
2007
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2346435/ https://ncbi.nlm.nih.gov/pubmed/18596842 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.tet.2007.03.016 |
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