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首页> 外文期刊>Journal of the American Chemical Society >Palladium-Catalyzed Coupling Reactions of Tetrafluoroethylene with Arylzinc Compounds
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Palladium-Catalyzed Coupling Reactions of Tetrafluoroethylene with Arylzinc Compounds

机译:四氟乙烯与芳基锌化合物的钯催化偶联反应

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摘要

Organofluorine compounds are widely used in all aspects of the chemical industry. Although tetrafluoroethylene (TFE) is an example of an economical bulk organofluorine feedstock, the use of TFE is mostly limited to the production of poly(tetrafluoroethylene) and copoly-mers with other alkenes. Furthermore, no catalytic transformation of TFE that involves carbon-fluorine bond activation has been reported to date. We herein report the first example of a palladium-catalyzed coupling reaction of TFE with arylzinc reagents in the presence of lithium iodide, giving α,β,β-trifluorostyrene derivatives in excellent yields.
机译:有机氟化合物广泛用于化学工业的各个方面。尽管四氟乙烯(TFE)是经济的本体有机氟原料的实例,但TFE的使用主要限于生产聚四氟乙烯和与其他烯烃的共聚体。此外,迄今为止尚未报道涉及碳-氟键活化的TFE的催化转化。我们在此报告了在碘化锂存在下,TFE与芳基锌试剂进行钯催化的偶联反应的第一个实例,从而以极高的收率得到α,β,β-三氟苯乙烯衍生物。

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  • 来源
    《Journal of the American Chemical Society》 |2011年第10期|p.3256-3259|共4页
  • 作者单位

    Department of Applied Chemistry, Faculty of Engineering, Osaka University, Suita, Osaka 565-0871, Japan Center for Atomic and Molecular Technologies, Osaka University, Suita, Osaka 565-0871, Japan;

    rnDepartment of Applied Chemistry, Faculty of Engineering, Osaka University, Suita, Osaka 565-0871, Japan;

    rnDepartment of Applied Chemistry, Faculty of Engineering, Osaka University, Suita, Osaka 565-0871, Japan;

    rnDepartment of Applied Chemistry, Faculty of Engineering, Osaka University, Suita, Osaka 565-0871, Japan;

    rnDepartment of Applied Chemistry, Faculty of Engineering, Osaka University, Suita, Osaka 565-0871, Japan;

    rnDepartment of Applied Chemistry, Faculty of Engineering, Osaka University, Suita, Osaka 565-0871, 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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