首页> 外文期刊>The Journal of Organic Chemistry >CuI-Catalyzed Suzuki—Miyaura and Sonogashira Cross-Coupling Reactions Using DABCO as Ligand
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CuI-Catalyzed Suzuki—Miyaura and Sonogashira Cross-Coupling Reactions Using DABCO as Ligand

机译:CuI催化的DABCO作为配体的Suzuki-Miyaura和Sonogashira交叉偶联反应

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摘要

In the presence of TBAB, CuI-catalyzed Suzuki—Miyaura cross-coupling of vinyl halides and aryl halides with arylboronic acids was conducted smoothly to afford the corresponding diarylethenes and polyaryls in moderate to good yields using DABCO (1,4-diazabicyclo[2.2.2]octane) as the ligand. We also found that the inexpensive CuI/DABCO catalytic system was effective for Sonogashira cross-couplings of aryl halides and vinyl halides. A variety of aryl halides and vinyl halides including activated aryl chlorides underwent the coupling with terminal alkynes in moderate to excellent yields.
机译:在TBAB存在下,使用DABCO(1,4-二氮杂双环[2.2。 2]辛烷)作为配体。我们还发现廉价的CuI / DABCO催化体系对于芳基卤化物和乙烯基卤化物的Sonogashira交叉偶联有效。各种芳基卤化物和乙烯基卤化物(包括活化的芳基氯化物)以中等至极好的收率与末端炔烃偶联。

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