首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >A convenient method for preparing aromatic ketones from acyl chlorides and arylboronic acids via Suzuki-Miyaura type coupling reaction
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A convenient method for preparing aromatic ketones from acyl chlorides and arylboronic acids via Suzuki-Miyaura type 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简便方法

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摘要

Aromatic ketones are synthesized efficiently via palladium-catalyzed cross-coupling reaction of boronic acids with acyl chlorides in the presence of K_3PO_4 hydrate in toluene. This allows the use of aliphatic acyl chlorides as the starting material. Hydrated water plays a significant role as an H_2O source to activate the catalytic system.
机译:在甲苯中存在K_3PO_4水合物时,硼酸与酰基氯的钯催化交叉偶联反应可有效合成芳族酮。这允许使用脂族酰氯作为起始原料。水合水作为激活催化系统的H_2O源发挥着重要作用。

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