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芳香酰氯和芳基硼酸的Suzuki-Miyaura偶联反应研究进展 被引量:1

Progress in Suzuki-Miyaura Cross-coupling Reaction of Aromatic Acyl Chloride and Aryl Boric Acid
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摘要 芳香酰氯具有较高的反应活性,易于和芳基硼酸反应生成工业上应用广泛的芳基酮。概述了应用各种钯催化剂,在条件温和、低毒的情况下进行芳香酰氯和芳基硼酸的Suzuki-Miyaura偶联反应,并就各类反应的优点进行了详细阐述。 Aromatic acyl chloride can easily react with aryl boric acids to give aryl ketones which are widely used in industry. The various kinds of palladium-catalyzed Suzuki-Miyaura coupling reactions of aromatic acyl chloride with aryl boric acid which were carried out under mild and low toxic reaction conditions were summarized in detail and the advantages of various kinds of reactions were elaborated.
出处 《化学世界》 CAS CSCD 北大核心 2013年第8期500-504,共5页 Chemical World
基金 山西省自然科学基金项目(2012021007-2 2011011010-2)
关键词 芳香酰氯 芳基硼酸 偶联 钯催化剂 aromatic acyl chloride aryl boric acid cross-coupling palladium catalyst
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