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Efficient Aryl-(Hetero)Aryl Coupling by Activation of C-Cl and C-F Bonds Using Nickel Complexes of Air-Stable Phosphine Oxides

机译:通过使用空气稳定的氧化膦的镍络合物活化C-Cl和C-F键来实现高效的芳基-(杂)芳基偶联

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摘要

Transition-metal-catalyzed cross-coupling reactions of orga-nomagnesium compounds are useful tools for the synthesis of unsymmetrically substituted biaryls,which are valuable building blocks for the synthesis of natural products,liquid crystals,polymers,and ligands.Predominantly aryl iodides and bromides,and more recently aryl chlorides,are employed as electrophiles.In contrast,the catalytic activation of unreactive C-F bonds remains extremely challenging because of the inherent strength of the C-F bond.The activation of C-F bonds in general is of utmost importance because this transformation contributes to the fundamental understanding of the reactivity of very stable bonds,and because the selective synthesis of partially fluorinated compounds is still a challenge.
机译:过渡金属催化的有机铝化合物的交叉偶联反应是合成不对称取代的联芳基的有用工具,它们是合成天然产物,液晶,聚合物和配体的有价值的组成部分。主要是芳基碘化物和溴化物相比之下,由于CF键的固有强度,未反应的CF键的催化活化仍然极具挑战性。CF键的活化通常极为重要,因为这种转化有助于对于非常稳定的键的反应性的基本理解,以及部分氟化化合物的选择性合成仍然是一个挑战。

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