首页> 外文期刊>Journal of the American Chemical Society >Ir(Ⅰ)-Catalyzed C-H Bond Alkylation of C2-Position of Indole with Alkenes: Selective Synthesis of Linear or Branched 2-Alkylindoles
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Ir(Ⅰ)-Catalyzed C-H Bond Alkylation of C2-Position of Indole with Alkenes: Selective Synthesis of Linear or Branched 2-Alkylindoles

机译:Ir(Ⅰ)催化的吲哚与烯烃的C2-位C-H键烷基化:线性或支化2-烷基炔醇的选择性合成

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摘要

A cationic iridium-catalyzed C2-alkylation of N-substituted indole derivatives with various alkenes has been developed, which selectively gives linear or branched 2-alkylindoles in high to excellent selectivity. This protocol relies on the use of the carbonyl group on the nitrogen atom of indole as a directing group: a linear product was predominant when an acetyl group was used as a directing group, and a branched product was predominant with a benzoyl group.
机译:已开发出具有各种烯烃的N-取代的吲哚衍生物的阳离子铱催化的C2-烷基化反应,该反应选择性地以高至优异的选择性生成直链或支链的2-烷基吲哚。该方案依赖于在吲哚的氮原子上使用羰基作为导向基团:当使用乙酰基作为导向基团时,线性产物占主导地位,而支链产物则以苯甲酰基为主。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2012年第42期|17474-17477|共4页
  • 作者单位

    Department of Chemistry and Biochemistry, School of Advanced Science and Engineering, Waseda University, Shinjuku, Tokyo,169-8555, Japan;

    Department of Chemistry and Biochemistry, School of Advanced Science and Engineering, Waseda University, Shinjuku, Tokyo,169-8555, Japan;

    Department of Chemistry and Biochemistry, School of Advanced Science and Engineering, Waseda University, Shinjuku, Tokyo,169-8555, Japan;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-18 03:13:38

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