Department of Chemistry and Biochemistry , Samford University , Birmingham , Alabama 35229 , United States.
J Org Chem. 2019 Sep 20;84(18):11612-11622. doi: 10.1021/acs.joc.9b01556. Epub 2019 Sep 4.
An operationally simple nickel-catalyzed hydroarylation reaction for alkynes is described. This three-component coupling reaction utilizes commercially available alkynes and aryl bromides, along with water and Zn. An air-stable and easily synthesized Ni(II) precatalyst is the only entity used in the reaction that is not commercially available. This reductive cross-coupling reaction displays a fairly unusual selectivity when aryl bromides with substituents are used. In addition to optimization data and a preliminary substrate scope, complementary experiments including deuterium labeling studies are used to provide a tentative catalytic mechanism. We believe this report should inspire and inform other Ni-catalyzed carbofunctionalization reactions.
描述了一种操作简单的镍催化炔烃的氢芳基化反应。该三组分偶联反应使用商业可得的炔烃和芳基溴化物以及水和 Zn。唯一未商品化的反应中使用的不是商业可得的空气稳定且易于合成的 Ni(II)前催化剂。当使用具有取代基的芳基溴化物时,这种还原交叉偶联反应表现出相当不寻常的选择性。除了优化数据和初步的底物范围外,还使用补充实验包括氘标记研究来提供暂定的催化机制。我们相信,本报告应该会激发和启发其他 Ni 催化的碳官能化反应。