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首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >Synthesis of 2,4-diarylimidazoles through suzuki cross-coupling reactions of imidazole halides with arylboronic acids
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Synthesis of 2,4-diarylimidazoles through suzuki cross-coupling reactions of imidazole halides with arylboronic acids

机译:咪唑卤化物与芳基硼酸的铃木交叉偶联反应合成2,4-二芳基咪唑

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摘要

The Suzuki coupling,a Pd-catalyzed cross-coupling reaction of a boronic acid with an aryl halide,was used to prepare several 2,4-diarylimidazoles.lodinated and brominated imidazoles (3) and (9) proved to be suitable aryl halides for Suzuki coupling.These imidazole halides readily reacted with phenyl-,naphthyl- and biphenylboronic acids under Suzuki conditions to give arylated imidazoles.
机译:Suzuki偶联是硼酸与芳基卤化物在Pd催化下的交叉偶联反应,用于制备几种2,4-二芳基咪唑。卤化和溴化的咪唑(3)和(9)被证明是适用于卤化芳基的芳基卤化物。在铃木条件下,这些咪唑卤化物很容易与苯基,萘基和联苯硼酸反应生成芳基化的咪唑。

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