首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Stereoselective construction of the ABC-ring system of fusidane triterpenes via intermolecular/transannular Michael reaction cascade
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Stereoselective construction of the ABC-ring system of fusidane triterpenes via intermolecular/transannular Michael reaction cascade

机译:分子间/跨环迈克尔反应级联的富丁烷三萜ABC环系统的立体选择性构建

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摘要

A stereoselective construction of the ABC-ring system of fusidane triterpenes via intermolecular/transannular Michael reaction cascade is described. The substrate, a ten-membered carbocyclic ketone, has been successfully prepared by the Cr-mediated intramolecular alkenylation of the corresponding acyclic compound. The array of functionalities in the product stereoselectively obtained by the cascade reaction is useful for further structural modifications directed toward the total synthesis of fusidane and other triterpenes, and designed molecules intended for studying structure-activity relationships.
机译:描述了通过分子间/跨环迈克尔反应级联的富丁烷三萜的ABC-环系统的立体选择性结构。通过相应的无环化合物的Cr介导的分子内烯基化已成功制备了十元碳环酮底物。通过级联反应立体选择性地获得的产物中的功能性阵列可用于进一步的修饰,这些修饰涉及夫西丹和其他三萜的全合成,以及设计用于研究结构与活性关系的分子。

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