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首页> 外文期刊>Synthesis: International Journal of Methods in Synthetic Organic Chemistry >An Efficient Copper(I) Iodide Catalyzed Synthesis of Diaryl Selenides through C_(Ar)-Se Bond Formation Using Solvent Acetonitrile as Ligand
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An Efficient Copper(I) Iodide Catalyzed Synthesis of Diaryl Selenides through C_(Ar)-Se Bond Formation Using Solvent Acetonitrile as Ligand

机译:以乙腈为配体的C_(Ar)-Se键形成高效碘化铜(I)催化合成二芳基硒化物

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摘要

A wide range of diaryl selenides can be synthesized through C_(Ar)-Se bond formation using readily available copper(I) iodide as catalyst under mild reaction conditions (82 degC) from aryl iodides and diphenyl diselenide. In this coupling reaction, solvent acetonitrile acts as ligand for copper(I) iodide and no external ligand is required. Less reactive aryl bromides also provide the diaryl selenides in good isolated yields.
机译:在适度的反应条件下(82摄氏度),使用碘化亚铜(I)作为催化剂,可以通过碘化亚铜和二苯基二硒化物通过C_(Ar)-Se键的形成,合成广泛的二芳基硒化物。在该偶联反应中,溶剂乙腈充当碘化亚铜(I)的配体,不需要外部配体。反应性较低的芳基溴化物也可以良好的分离产率提供二芳基硒化物。

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