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Fused ring aziridines as a facile entry into triazole fused tricyclic and bicyclic heterocycles

机译:稠合环氮丙啶类化合物可轻松进入三唑稠合的三环和双环杂环

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摘要

The intramolecular dipolar cycloaddition of an azide with an alkyne has provided a useful entry into triazole fused tricyclic heterocycles containing both the triazole ring and the oxazolidin-2-one ring system. The requisite azido-alkynes have been prepared via a two-step sequence from fused ring aziridines. A series of 6-12 membered rings containing both the oxazolidinone and triazole rings have been prepared. These ring systems have been designed as conformationally restrained analogs of RNA-binding oxazolidinones.
机译:叠氮化物与炔烃的分子内偶极环加成为包含三唑环和恶唑烷-2-一环系统的三唑稠合的三环杂环提供了有用的入口。必需的叠氮基-炔烃已通过两步序列由稠合环氮丙啶制备。已经制备了一系列同时含有恶唑烷酮和三唑环的6-12元环。这些环系统已被设计为结合RNA的恶唑烷酮的构象受限类似物。

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  • 来源
    《Organic & biomolecular chemistry》 |2012年第15期|p.3080-3091|共12页
  • 作者单位

    Clippinger Laboratory, Department of Chemistry and Biochemistry, Ohio University, Athens, OH45701, USA;

    Clippinger Laboratory, Department of Chemistry and Biochemistry, Ohio University, Athens, OH45701, USA;

    Clippinger Laboratory, Department of Chemistry and Biochemistry, Ohio University, Athens, OH45701, USA;

    Clippinger Laboratory, Department of Chemistry and Biochemistry, Ohio University, Athens, OH45701, USA;

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