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Rational development of catalytic Au(I)/Au(III) arylation involving mild oxidative addition of aryl halides

机译:合理开发Au(I)/ Au(III)催化芳基化反应涉及轻度氧化添加芳基卤化物

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摘要

The reluctance of gold to achieve oxidative addition reaction is considered as an intrinsic limitation for the development of gold-catalyzed cross-coupling reactions with simple and ubiquitous aryl halide electrophiles. Here, we report the rational construction of a Au(I)/Au(III) catalytic cycle involving a sequence of Csp2–X oxidative addition, Csp2–H auration and reductive elimination, allowing a gold-catalyzed direct arylation of arenes with aryl halides. Key to this discovery is the use of Me-Dalphos, a simple ancillary (P,N) ligand, that allows the bottleneck oxidative addition of aryl iodides and bromides to readily proceed under mild conditions. The hemilabile character of the amino group plays a crucial role in this transformation, as substantiated by density functional theory calculations.
机译:金不愿实现氧化加成反应被认为是开发具有简单且普遍存在的芳基卤化亲电试剂的金催化交叉偶联反应的固有限制。在这里,我们报告了Aus(I)/ Au(III)催化循环的合理构建,该循环涉及一系列Csp 2 -X氧化加成,Csp 2 -H氧化还原性消除,使金与芳基卤化物直接催化芳烃的芳基化。该发现的关键是使用Me-Dalphos(一种简单的辅助(P,N)配体),该化合物可以在温和条件下容易地进行芳基碘和溴化物的瓶颈氧化加成。如密度泛函理论计算所证实的,氨基的半不稳定特性在这种转变中起着至关重要的作用。

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