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Selective coupling reaction between 2,6-diiodoanisoles and terminal alkynes catalyzed by Pd(PPh3)2Cl2 and CuI

机译:Pd(PPh3)2Cl2和CuI催化2,6-二碘苯甲醚与末端炔烃的选择性偶联反应

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The cross-coupling reaction between aryl halides and terminal alkynes, catalyzed by palladium complexes and copper (I) salts, consists in an efficient synthetic tool for the formation of C-C bonds, resulting in disubstituted acetylenic compounds. Accordingly, in this work we present our preliminary results involving the selective cross-coupling reaction between 2,6-diiodoanisoles and terminal alkynes, catalyzed by Pd(PPh3)2Cl2 and CuI, in the formation of 2-iodo-alkynylanisoles (scheme 1).
机译:钯配合物和铜(I)盐催化的芳基卤化物与末端炔烃之间的交叉偶联反应,是形成C-C键的有效合成工具,可生成二取代的炔属化合物。因此,在这项工作中,我们提出了初步的结果,涉及在Pd(PPh3)2Cl2和CuI的催化下,2-碘二碘苯甲醚与末端炔烃的选择性交叉偶联反应,形成了2-碘炔基苯甲醚(方案1)。 。

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