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Synthesis of cananodine by intramolecular epoxide opening
Cananodine is a guaipyridine alkaloid with activity against liver cancer. Cananodine was synthesized using a remarkable intramolecular opening of a trisubstituted epoxide as the key step in construction of the seven-membered carbocycle of the target. The epoxide opening strategy allows all four ster...
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| Vydáno v: | Tetrahedron Lett |
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| Hlavní autoři: | , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2017
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5722248/ https://ncbi.nlm.nih.gov/pubmed/29230072 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.tetlet.2017.07.080 |
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