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Ruthenium-Catalyzed Transformation of Aryl and Alkenyl Triflates to Halides

机译:钌催化的芳基和烯基三氟甲磺酸盐转化为卤化物

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摘要

Aryl triflates were transformed to aryl bromides/iodides simply by treating them with LiBr/Nal and [Cp~*Ru(MeCN)_3]OTf. The ruthenium complex also catalyzed the transformation of alkenyl sulfonates and phosphates to alkenyl halides under mild conditions. Aryl and alkenyl triflates undergo oxidative addition to a ruthenium(Ⅱ) complex to form η~1-arylruthenium and 1-ruthenacyclopropene intermediates, respectively, which are transformed to the corresponding halides.
机译:只需用LiBr / Nal和[Cp〜* Ru(MeCN)_3] OTf处理,即可将芳基三氟甲磺酸酯转化为芳基溴化物/碘化物。在温和的条件下,钌络合物还催化了烯基磺酸盐和磷酸盐的转化为烯基卤化物。芳基和烯基三氟甲磺酸酯经过氧化加成到钌(Ⅱ)配合物中,分别形成η〜1-芳基钌和1-钌环丙烯中间体,然后转化为相应的卤化物。

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  • 来源
    《Journal of the American Chemical Society》 |2012年第36期|p.14760-14763|共4页
  • 作者单位

    Department of Chemistry, Graduate School of Science, Kyoto University, Sakyo, Kyoto 606-8502, Japan;

    Department of Chemistry, Graduate School of Science, Kyoto University, Sakyo, Kyoto 606-8502, Japan;

    Department of Chemistry, Graduate School of Science, Kyoto University, Sakyo, Kyoto 606-8502, Japan;

    Department of Chemistry, Graduate School of Science, Kyoto University, Sakyo, Kyoto 606-8502, Japan;

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