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Ni-Catalyzed Arylboration of Unactivated Alkenes: Scope and Mechanistic Studies

机译:Ni催化的芳族芳硼酸盐:范围和机械研究

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摘要

A method for the Ni-catalyzed arylboration of unactivated monosubstituted, 1,1-disubstituted, and trisubstituted alkenes is disclosed. The reaction is notable in that it converts highly substituted alkenes, aryl bromides, and diboron reagents to products that contain a quaternary carbon and a synthetically versatile carbon boron bond with control of stereoselectivity and regioselectivity. In addition, the method is demonstrated to be useful for the synthesis of saturated nitrogen heterocycles, which are important motifs in pharmaceutical compounds. Finally, due to the unusual reactivity demonstrated, the mechanistic details of the reaction were studied with both computational and experimental techniques.
机译:公开了一种Ni催化的单取代剂,1,1-二取代和三取代烯烃的Ni催化芳基硼酸盐的方法。该反应非常值得注于,它将高度取代的烯烃,芳族溴化物和二硼试剂转化为含有季碳和合成通用碳硼键的产物,其具有控制立体选择性和区域选择性。此外,证明该方法可用于合成饱和氮杂环,其是药物化合物中的重要基序。最后,由于表现出不寻常的反应性,通过计算和实验技术研究了反应的机械细节。

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  • 来源
    《Journal of the American Chemical Society》 |2019年第23期|9391-9400|共10页
  • 作者单位

    Indiana Univ Dept Chem 800 East Kirkwood Ave Bloomington IN 47405 USA;

    Indiana Univ Dept Chem 800 East Kirkwood Ave Bloomington IN 47405 USA;

    Indiana Univ Dept Chem 800 East Kirkwood Ave Bloomington IN 47405 USA;

    Univ Pittsburgh Dept Chem 219 Parkman Ave Pittsburgh PA 15260 USA;

    Univ Pittsburgh Dept Chem 219 Parkman Ave Pittsburgh PA 15260 USA;

    Indiana Univ Dept Chem 800 East Kirkwood Ave Bloomington IN 47405 USA;

  • 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);
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  • 正文语种 eng
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