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Rh-III-Catalyzed Synthesis of Cyclopenta[b]carbazoles via Cascade C-H/C-C Bond Cleavage and Cyclization Reactions: Using Amide as a Traceless Directing Group

机译:RH-III催化的环戊基合成通过级联C-H / C-C键切割和环化反应:使用酰胺作为无痕指示组

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摘要

Rhodium-catalyzed cascade C-H/C-C cleavage and cyclization reactions of 3-amide substituted indoles with diynes to construct cyclopenta[b]carbazoles have been developed. A strategy amide worked as a novel traceless directing group along with C-C bond cleavage via Friedel-Crafts-retro reaction has been disclosed in this protocol. This method exhibits a broad substrate scope and tolerates various functional groups, furnishing the carbazole derivatives in good to high yields.
机译:铑催化的级联C-H / C-C裂解和三酰胺取代吲哚与DIYNES构建环戊基[B]咔唑的C-H / C-C裂解和环化反应。 通过Friedel-Crafts-Recro反应在本方案中公开了一种策略作为一种新颖的无缺陷指示组以及C-C键的切割。 该方法表现出宽的基材范围并耐受各种官能团,良好地提供咔唑衍生物的高产率。

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  • 来源
    《Organic letters》 |2020年第1期|共5页
  • 作者单位

    Nankai Univ State Key Lab Elementoorgan Chem Coll Chem Tianjin 300071 Peoples R China;

    Nankai Univ State Key Lab Elementoorgan Chem Coll Chem Tianjin 300071 Peoples R China;

    Nankai Univ State Key Lab Elementoorgan Chem Coll Chem Tianjin 300071 Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 有机化学;
  • 关键词

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