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首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >A rapid,solvent-free,ligandless and mild method for preparing aromatic ketones from acyl chlorides and arylboronic acids via a Suzuki-Miyaura type of coupling reaction
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A rapid,solvent-free,ligandless and mild method for preparing aromatic ketones from acyl chlorides and arylboronic acids via a Suzuki-Miyaura type of coupling reaction

机译:通过Suzuki-Miyaura型偶联反应从酰氯和芳基硼酸制备芳族酮的快速,无溶剂,无配体且温和的方法

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摘要

Aromatic ketones were synthesized via a palladium catalyzed cross-coupling reaction of boronic acids with acyl chlorides in the presence of Na_2CO_3 at room temperature under solvent-free conditions.The Iigand-free and mild reaction conditions,highly rapid reaction rate and good to excellent yields are important features of this method.
机译:在室温,无溶剂条件下,在Na_2CO_3存在下,硼酸与酰基氯的钯催化交叉偶联反应合成芳族酮。无配体且反应条件温和,反应速度快,收率良好,具有优异的收率是此方法的重要功能。

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