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Synthesis of (±)-Eusynstyelamide A

[Image: see text] The synthesis of (±)-eusynstyelamide A has been accomplished in six steps in 13% overall yield from 6-bromoindole, methyl glycidate, and Boc-protected agmatine. If oxygen is carefully excluded from the reaction, the key NaOH-catalyzed aldol dimerization of the α-ketoamide proceeded...

詳細記述

保存先:
書誌詳細
主要な著者: Barykina, Olga V., Snider, Barry B.
フォーマット: Artigo
言語:Inglês
出版事項: 2010
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC2878381/
https://ncbi.nlm.nih.gov/pubmed/20446668
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/ol100896n
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