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首页> 外文期刊>Catalysis Communications >Oxygen-promoted Suzuki-Miyaura reaction of aryl fluorosulfates and potassium aryltrifluoroborates: Mild and efficient access to biaryls and terphenyls
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Oxygen-promoted Suzuki-Miyaura reaction of aryl fluorosulfates and potassium aryltrifluoroborates: Mild and efficient access to biaryls and terphenyls

机译:氧氟磺酸盐和芳基三氟硼酸钾的氧促进的铃木 - 宫系反应:轻度和有效地进入芳基团和三苯基

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摘要

A mild and efficient protocol has been developed for the Suzuki-Miyaura reaction of aryl fluorosulfates and potassium aryltrifluoroborates at room temperature. A series of biaryls can be prepared with excellent yields in this system and an aerobic atmosphere demonstrates a positive effect on the reactivity of the cross-coupling reactions. Additionally, this method can be extended to one-pot double Suzuki-Miyaura reactions, allowing the synthesis of various unsymmetrical terphenyls in moderate to good yields.
机译:已经为芳基氟磺酸盐和芳基三氟硼硼酸钾在室温下进行了温和和高效的方案。 可以在该系统中具有优异产量的一系列前列,并且有氧气氛证明了对交叉偶联反应的反应性的积极影响。 另外,该方法可以扩展到单盆双铃木 - Miyaura反应,允许在中等至良好的产率中合成各种非对称的三苯基。

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