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Iron-Catalyzed Direct Arylation of Unactivated Arenes with Aryl Halides

机译:未活化的芳烃与芳基卤化物的铁催化直接芳基化

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摘要

Cross-coupling reactions used to construct biaryl compounds mainly involve Ar~1X as an electrophile and Ar~2M as a nucleophile. Recently, C-H bond activation has been used, where Ar~2H served as the nucleophile to react with Ar~1X (direct arylation of arenes). This strategy efficiently avoids the disposal of stoichiometric amounts of metal waste generated from the organometallic reagent, ArM, in the traditional coupling manner. Various transition metals have been reported as efficient catalysts for this transformation, for example, Pd, Rh, Ru, Ir, Cu, and other transition metals.
机译:用于构建联芳基化合物的交叉偶联反应主要涉及Ar〜1X作为亲电子试剂和Ar〜2M作为亲核试剂。近来,已使用C-H键活化,其中Ar〜2H充当亲核试剂以与Ar〜1X(芳烃的直接芳基化)反应。该策略有效地避免了以传统的偶联方式处理化学计量的有机金属试剂ArM产生的金属废物。已经报道了各种过渡金属作为该转化的有效催化剂,例如Pd,Rh,Ru,Ir,Cu和其他过渡金属。

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