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钯催化的炔丙基溴化物的 domino 环化反应合成稠合和连接的双环氮杂环。

Synthesis of fused and linked bicyclic nitrogen heterocycles by palladium-catalyzed domino cyclization of propargyl bromides.

机构信息

Graduate School of Pharmaceutical Sciences, Kyoto University, Sakyo-ku, Kyoto 606-8501, Japan.

出版信息

Chemistry. 2010 Jul 26;16(28):8410-8. doi: 10.1002/chem.201000653.

Abstract

The palladium(0)-catalyzed direct construction of bicyclic heterocycles is described. Treatment of propargyl bromides that have nucleophilic functional groups connected by two or three carbon atoms with catalytic [Pd(PPh(3))(4)] affords bis-cyclization products in good yields. The desired bicyclic heterocycles can be obtained selectively when using substrates with appropriate nucleophilic groups. We also describe the reaction of a 2-alkynylazetidine derivative with a catalytic amount of [Pd(PPh(3))(4)] under base-free conditions, which affords the same fused heterocycles as the corresponding propargyl bromides.

摘要

描述了钯(0)催化的双环杂环的直接构建。用催化量的[Pd(PPh3)4]处理具有通过两个或三个碳原子连接的亲核官能团的炔丙基溴化物,可得到双环化产物,产率良好。当使用具有适当亲核基团的底物时,可以选择性地得到所需的双环杂环。我们还描述了在无碱条件下,用催化量的[Pd(PPh3)4]处理 2-炔基氮杂环丁烷衍生物的反应,得到与相应的炔丙基溴化物相同的稠合杂环。

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