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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Bibliografiske detaljer
Main Authors: Han, Seo-Jung, Vogt, Florian, Krishnan, Shyam, May, Jeremy A., Gatti, Michele, Virgil, Scott C., Stoltz, Brian M.
Format: Artigo
Sprog:Inglês
Udgivet: American Chemical Society 2014
Online adgang: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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