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Nickel-catalyzed cross-coupling reactions of 4-mesylcoumarins with aryl halides: Facile synthesis of 4-substituted coumarins

机译:4-甲磺酰香豆素与芳基卤化物的镍催化交叉偶联反应:4-取代香豆素的简便合成

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摘要

A new and efficient nickel-catalyzed cross-coupling reaction between 4-mesylcoumarins and aryl halides was developed to give a number of 4-arylcoumarins in good yield under mild conditions. Unlike the previously reported coupling examples, this new method allows the direct cross-coupling of 4-mesylcoumarins with aryl- or vinyl halides in the NiCl2(PPh3)(2)/PPh3/Zn/toluene system. This has greatly facilitated the synthesis of biologically useful 4-substituted coumarins.
机译:开发了一种新的高效的4-甲磺酰基香豆素与芳基卤化物之间的镍催化交叉偶联反应,可在温和条件下以良好的收率得到许多4-芳基香豆素。与以前报道的偶合实例不同,这种新方法允许在NiCl2(PPh3)(2)/ PPh3 / Zn /甲苯系统中将4-甲磺酰基香豆素与芳基或乙烯基卤化物直接交叉偶合。这极大地促进了生物学上有用的4-取代的香豆素的合成。

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