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Divergent Synthesis of Quinolone Natural Products from Pseudonocardia sp. CL38489
Two divergent synthetic routes are reported offering access to four quinolone natural products from Pseudonocardia sp. CL38489. Key steps to the natural products involved a regioselective epoxidation, an intramolecular Buchwald–Hartwig amination and a final acid‐catalysed 1,3‐allylic‐alcohol rearran...
Tallennettuna:
| Julkaisussa: | European J Org Chem |
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| Päätekijät: | , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
John Wiley and Sons Inc.
2016
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5215369/ https://ncbi.nlm.nih.gov/pubmed/28111524 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ejoc.201601195 |
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