用IMDA反应合成一种天然聚蜜苷类似物

Jean-François Betzer, Janick Ardisson, Ange Pancrazi
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引用次数: 0

摘要

在我们的新大环抗生素衍生物合成计划中,分离到一种天然的菊胺霉素类似物,揭示了重要的抗生素和抗病毒特性,正在研究中。本文描述了它的下半部分C1-C14 (n = 1)的合成。该策略基于钯催化Stille偶联反应制备四烯衍生物,最后一步涉及IMDA环化的关键步骤。
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IMDA reaction in a synthetic approach towards a natural kijamicin aglycon analog

In our program of new macrocyclic antibiotic derivatives synthesis, a natural kijamicin analog was isolated, disclosing important antibiotic and antiviral properties, which are under investigation. In this paper we describe a synthesis of the bottom half C1-C14 (n = 1) of its aglycon. This strategy was based on the preparation of a tetraene derivative via a palladium catalyzed Stille coupling reaction, the final step involving an IMDA cyclization key step.

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