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Nickel-Catalyzed Electrochemical Reductive Homocouplings of Aryl and Heteroaryl Halides: A Useful Route to Symmetrical Biaryls

机译:芳基的镍催化电化学还原性同性环节和杂芳基卤化物:对称前列的有用途径

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摘要

Due to their widespread presence in functional materials and pharmaceuticals, biaryls are of fundamental importance in organic chemistry. Methods for the synthesis of symmetrical biaryls generally involve both metallic reduction and transition-metal catalysis. In this work, we show that electroreduction can also constitute a very relevant way to achieve the nickel-catalyzed reductive synthesis of symmetrical biaryl compounds. Therefore, it is demonstrated that both aryl and heteroaryl halides undergo reductive coupling to furnish the corresponding symmetrical biaryls in fair to excellent yields. Reactions are performed under very mild conditions thus ensuring important functional group tolerance.
机译:由于其在功能材料和药物中的广泛存在,野生醛在有机化学中具有根本重要性。 合成对称纤维素的方法通常涉及金属还原和过渡金属催化。 在这项工作中,我们表明,电荷还可以构成实现对称芳基化合物的镍催化的还原合成的非常相关的方法。 因此,证明了芳基和杂芳基卤化物经过还原偶联,以将相应的对称纤维素提供优异的产率。 反应在非常温和的条件下进行,从而确保重要的官能团耐受性。

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