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Nickel-Catalyzed Decarbonylative Alkylidenation of Phthalimides with Trimethylsilyl-Substituted Alkynes

机译:邻苯二甲酰亚胺与三甲基甲硅烷基取代的炔烃的镍催化脱羰烷基化

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摘要

We have developed a nickel-catalyzed transformation, in which phthalimides react with trime-thylsilyl-substituted alkynes in the presence of Ni(0)/ PMe_3/MAD catalyst to provide isoindolinones. The reaction process displays an unusual mechanistic feature-decarbonylation and alkylidenation. The use of both trimethylsilyl-substiuted alkynes and MAD was found to be essential for the transformation with high selectivities.
机译:我们已经开发了镍催化的转化,其中邻苯二甲酰亚胺在Ni(0)/ PMe_3 / MAD催化剂存在下与偏苯三甲硅烷基取代的炔烃反应以提供异吲哚啉酮。反应过程显示出异常的机理特征-脱羰基和亚烷基化。发现同时使用三甲基甲硅烷基取代的炔烃和MAD对于高选择性转化至关重要。

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  • 来源
    《Journal of the American Chemical Society》 |2013年第37期|13636-13639|共4页
  • 作者单位

    Department of Material Chemistry, Graduate School of Engineering, Kyoto University, Kyoto 615-8510, Japan;

    Department of Material Chemistry, Graduate School of Engineering, Kyoto University, Kyoto 615-8510, Japan,JST, ACT-C, Saitama, 332-0012, Japan;

    Department of Material Chemistry, Graduate School of Engineering, Kyoto University, Kyoto 615-8510, 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);
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  • 正文语种 eng
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