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Biaryl Cross-Coupling Reactions Controlled by Fluoride Ion and Bulky Monodentate Ligands

机译:由氟离子和庞大的单齿配体控制的Biaryl交叉偶联反应

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The transition metal-catalyzed cross-coupling reaction is a powerful tool for selective synthesis of unsymmetrical biaryls. Among widely studied and utilized aryl metal reagents, such as aryl magnesium, zinc, copper, tin, silicon, aluminum, lithium, and boron compounds, aryl magnesium reagents are the most economical and versatile in terms of the practicality of biaryl synthesis. There have been, however, only a few industrial applications of unsymmetrical biaryl synthesis due to considerable formation of the byproduct symmetrical biaryls via the undesired homo-coupling reactions. Herein, we report simple and highly selective biaryl couplings based on iron, cobalt, and nickel-catalysts by the aid of a rather unconventional ligand combination; a fluoride anion and a bulky monodentate ligand.
机译:过渡金属催化的交叉偶联反应是用于选择性合成非对称前列的强大工具。在普遍研究和使用的芳基金属试剂中,例如芳基镁,铜,铜,锡,硅,铝,锂和硼化合物,芳基镁试剂是芳基合成的实用性最经济和多功能的。然而,已经仅通过不需要的均偶联反应显着形成副产物对称纤维素的少量非对称的辅导合成的工业应用。在此,我们通过借助于相当非常规的配体组合报告基于铁,钴和镍催化剂的简单且高度选择性的辅导偶联;氟化物阴离子和庞大的单张配体。

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