首页> 外文期刊>The Journal of Organic Chemistry >Decarboxylative Halogenation and Cyanation of Electron-Deficient Aryl Carboxylic Acids via Cu Mediator as Well as Electron-Rich Ones through Pd Catalyst under Aerobic Conditions
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Decarboxylative Halogenation and Cyanation of Electron-Deficient Aryl Carboxylic Acids via Cu Mediator as Well as Electron-Rich Ones through Pd Catalyst under Aerobic Conditions

机译:有氧条件下通过铜介体以及富电子的Pd催化剂对缺电子的芳基羧酸进行脱羧卤化和氰化

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摘要

Simple strategies for decarboxylative functionalizations of electron-deficient benzoic acids via using Cu(I) as promoter and electron-rich ones by employing Pd(II) as catalyst under aerobic conditions have been established, which lead to smooth synthesis of aryl halides (-I, Br, and Cl) through the decarboxylative functionalization of benzoic acids with readily available halogen sources CuX (X = I, Br, Cl), and easy preparation of benzonitriles from decarboxylative cyanation of aryl carboxylic acids with nontoxic and low-cost K4Fe(CN)(6) under an oxygen atmosphere for the first time.
机译:建立了一种简单的策略,在需氧条件下,通过使用Cu(I)作为促进剂和富电子的Pd(II)作为催化剂,对缺电子的苯甲酸进行脱羧功能化,从而导致芳基卤化物(-I)的顺利合成,Br和Cl),通过使用容易获得的卤素源CuX(X = I,Br,Cl)对苯甲酸进行脱羧功能化,以及通过使用无毒和低成本K4Fe(CN)的芳基羧酸的脱羧氰化反应轻松制备苄腈)(6)首次在氧气气氛下。

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