Karpova Lidia, Daniel Matěj, Kancherla Rajesh, Muralirajan Krishnamoorthy, Maity Bholanath, Rueping Magnus
Kaust Catalysis Center (KCC), King Abdullah University of Science and Technology (KAUST), Thuwal 23955-6900, Saudi Arabia.
Org Lett. 2024 Mar 1;26(8):1657-1661. doi: 10.1021/acs.orglett.4c00147. Epub 2024 Feb 21.
Excited-state nickel-catalyzed C-N cross-coupling of aryl bromides with sodium azide enables the synthesis of diarylamines and primary anilines under mild reaction conditions. The oxidative addition of electron-rich aryl bromides with low-valent Ni under the photochemical conditions is endothermic. Herein, we demonstrate a light-mediated nickel-catalyzed reaction of electronically rich aryl bromides that yields diarylamines, while the reaction with electron-deficient aryl bromides gives access to anilines at room temperature.
激发态镍催化芳基溴化物与叠氮化钠的C-N交叉偶联反应能够在温和的反应条件下合成二芳基胺和伯苯胺。在光化学条件下,富电子芳基溴化物与低价镍的氧化加成反应是吸热的。在此,我们展示了一种光介导的镍催化富电子芳基溴化物反应,该反应可生成二芳基胺,而与缺电子芳基溴化物的反应则能在室温下得到苯胺。