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首页> 外文期刊>The Journal of Organic Chemistry >Skeletal diverse synthesis of N-fused polycyclic heterocycles via the sequence of Ugi-type MCR and CuI-catalyzed coupling/tandem Pictet-Spengler reaction
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Skeletal diverse synthesis of N-fused polycyclic heterocycles via the sequence of Ugi-type MCR and CuI-catalyzed coupling/tandem Pictet-Spengler reaction

机译:通过Ugi型MCR和CuI催化的偶联/串联Pictet-Spengler反应的序列,N稠合多环杂环的骨架多样化合成

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摘要

Several diversity-oriented syntheses of N-fused polycyclic heterocycles have been demonstrated but most of them are based on point diversity within the same library and usually involve time-consuming sequential multistep syntheses, which also suffer from low yields and/or poor precursor scopes. We have developed a new strategy for the syntheses of skeletal diverse N-fused polycyclic compounds via an Ugi-type MCR followed by a CuI-catalyzed coupling reaction or tandem Pictet-Spengler reaction. This two-step sequence provides eight distinct skeleton of fused {6-5-5-6
机译:已经证明了N-稠合多环杂环的几种面向多样性的合成方法,但大多数基于同一库中的点多样性,并且通常涉及耗时的连续多步合成,这也具有产率低和/或前驱物范围差的缺点。我们已经开发出一种新的策略,可通过Ugi型MCR,然后由CuI催化的偶联反应或串联Pictet-Spengler反应合成骨架多样的N稠合多环化合物。这两个步骤的序列提供了融合{6-5-5-6

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