bengamide-e has been researched along with tartaric-acid* in 1 studies
1 other study(ies) available for bengamide-e and tartaric-acid
Article | Year |
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Enantiospecific total synthesis of (-)-bengamide E.
Total synthesis of the polyhydroxy caprolactam amide natural product, bengamide E, is accomplished starting from tartaric acid. Key reactions in the synthesis include desymmetrization of the bis(dimethylamide) unit of tartaric acid, Zn(BH(4))(2)-mediated anti-selective reduction, and a Horner-Wadsworth-Emmons olefination. Topics: Alkenes; Amides; Azepines; Caprolactam; Stereoisomerism; Tartrates | 2013 |