首页> 外文会议>Symposium on Organometallic Chemistry >Synthesis of Perfluoroalkylated Benzenes and Pyridines through Cationic Rh(I)/Modified-BINAP-Catalyzed Chemo- and Regioselective 2 + 2 + 2 Cycloaddition
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Synthesis of Perfluoroalkylated Benzenes and Pyridines through Cationic Rh(I)/Modified-BINAP-Catalyzed Chemo- and Regioselective 2 + 2 + 2 Cycloaddition

机译:通过阳离子RH(I)/改性-Binap催化的化学和区域选择性的全氟烷基苯并合成吡啶和吡啶2 + 2 + 2环加成

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Perfluoroalkylated aromatic compounds are important building blocks for the synthesis of various catalysts,reagents,and substrates used for fluorous chemistry,so the development of their convenient synthetic methods is highly desired.The most frequently employed regioselective method is a Cu-mediated cross-coupling reaction of perfluoroalkyl iodides and aryl halides developed by McLoughlin and Thrower.However,this method requires harsh reaction conditions,excess Cu-reagents,and regioselective preparation of the aryl halides.
机译:全氟烷基化的芳族化合物是用于合成各种催化剂,试剂和用于流氟化学的基材的重要组成块,因此非常需要开发其方便的合成方法。最常使用的区域选择性方法是Cu介导的交叉偶联反应通过Mcloughlin和推动力产生的全氟烷基碘和芳基卤化物。然而,该方法需要苛刻的反应条件,过量的Cu-试剂和芳基卤化物的区域选择性制备。

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