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首页> 外文期刊>Journal of Fluorine Chemistry >Efficient synthesis of fluorinated biphenyl derivatives via Pd-catalyzed Suzuki coupling reactions in aqueous solvents at room temperature
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Efficient synthesis of fluorinated biphenyl derivatives via Pd-catalyzed Suzuki coupling reactions in aqueous solvents at room temperature

机译:在室温下在水性溶剂中通过Pd催化的Suzuki偶联反应高效合成氟化联苯衍生物

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摘要

A variety of fluorinated biphenyl derivatives were obtained in good yields in aqueous solvents at room temperature by Suzuki coupling reaction of aryl bromides and aryl boronic acid in the presence of high activity catalyst-some air-stable hemilabile P-O coordinated cyclopalladated complexes.The structures of above catalysts were characterized by element analyses,IR,~H NMR,~(13)C NMR and ~(31)P NMR.
机译:在高活性催化剂-一些空气稳定的半不稳定的PO配位的环钯配合物的存在下,芳基溴化物和芳基硼​​酸的Suzuki偶联反应可在室温下在水性溶剂中以高收率获得多种氟化联苯衍生物。通过元素分析,IR,〜1 H NMR,〜(13)C NMR和〜(31)P NMR表征催化剂。

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