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A Diastereodivergent Synthetic Strategy for the Syntheses of Communesin F and Perophoramidine
[Image: see text] An efficient, unified, and stereodivergent approach toward communesin F and perophoramidine was examined. The C(3) all-carbon quaternary center of an oxindole was smoothly constructed by base-promoted indolone-malonate alkylation chemistry. The complementary relative stereochemistr...
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| Autori principali: | , , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
American Chemical Society
2014
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| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4068777/ https://ncbi.nlm.nih.gov/pubmed/24909760 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/ol5013263 |
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