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TfOH-catalyzed synthesis of 3-aryl isoindolinones via a tandem reaction

机译:TfOH催化串联反应合成3-芳基异吲哚满酮

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摘要

A convenient metal-free method for the synthesis of 3-aryl isoindolinones via TfOH catalyzed aromatic C-H functionalization of electron-rich arenes with 2-formylbenzonitriles is developed. This process provided a new efficient strategy for the synthesis of isoindolinone derivatives in good to high yields and regioselectivities by forming two bonds.
机译:开发了一种方便的无金属方法,该方法可通过TfOH催化富电子芳烃与2-甲酰基苄腈的芳族C-H官能化反应来合成3-芳基异吲哚啉酮。该方法为合成异吲哚啉酮衍生物提供了一个新的有效策略,该方法可通过形成两个键以高产率,高区域选择性和高选择性合成异吲哚啉酮衍生物。

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  • 来源
    《Chemical Communications》 |2014年第99期|15780-15783|共4页
  • 作者单位

    Department of Pharmaceutical Engineering, Wuhan University of Technology, Wuhan, 430070, China;

    Department of Pharmaceutical Engineering, Wuhan University of Technology, Wuhan, 430070, China;

    Department of Pharmaceutical Engineering, Wuhan University of Technology, Wuhan, 430070, China;

    Department of Pharmaceutical Engineering, Wuhan University of Technology, Wuhan, 430070, China;

    Department of Pharmaceutical Engineering, Wuhan University of Technology, Wuhan, 430070, China;

    Department of Pharmaceutical Engineering, Wuhan University of Technology, Wuhan, 430070, China;

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