首页> 外文期刊>Journal of the American Chemical Society >Tuning Reactivity and Site Selectivity of Simple Arenes in C-H Activation: Ortho-Arylation of Anisoles via Arene-Metal π-Complexation
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Tuning Reactivity and Site Selectivity of Simple Arenes in C-H Activation: Ortho-Arylation of Anisoles via Arene-Metal π-Complexation

机译:调节C-H活化中简单芳烃的反应性和位点选择性:通过芳族金属π-络合物对异氰酸酯进行邻位芳基化

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摘要

Current approaches to achieve site selectivity in the C-H activation of arenes involve the use of directing groups or highly electron-poor arenes. In contrast, simple arenes, such as anisole, are characterized by poor reactivity and selectivity. We report that π-complexation to a Cr(CO)_3 unit enhances the reactivity of anisoles providing an unprecedented ortho-selective arylation. This mild methodology can be used for the late stage functionalization of bioactive compounds containing the anisole motif, allowing the construction of novel organic scaffolds with few synthetic steps.
机译:当前在芳烃的C-H活化中实现位点选择性的方法涉及使用导向基团或电子贫乏的芳烃。相反,诸如苯甲醚之类的简单芳烃的特征是反应性和选择性差。我们报告到Cr(CO)_3单元的π络合物增强了提供空前的邻位选择性芳构化的各向异性的反应性。这种温和的方法可以用于含苯甲醚基序的生物活性化合物的后期功能化,从而使合成步骤很少的新型有机支架得以构建。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2014年第52期|18082-18086|共5页
  • 作者单位

    School of Biological and Chemical Sciences, Queen Mary University of London, Joseph Priestley Building, Mile End Road, E1 4NS, London, U.K.,School of Chemistry, University of Manchester, Oxford Road, Manchester, M13 9PL, U.K.;

    School of Biological and Chemical Sciences, Queen Mary University of London, Joseph Priestley Building, Mile End Road, E1 4NS, London, U.K.;

    School of Chemistry, University of Manchester, Oxford Road, Manchester, M13 9PL, U.K.;

  • 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 03:11:24

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