Nickel-Catalyzed Heteroarenes Cross Coupling via Tandem C–H/C–O Activation
作者:Ting-Hsuan Wang、Ram Ambre、Qing Wang、Wei-Chih Lee、Pen-Cheng Wang、Yuhua Liu、Lili Zhao、Tiow-Gan Ong
DOI:10.1021/acscatal.8b03436
日期:2018.12.7
Inert aryl methyl ethers as coupling components via C–O activation have been established with a Ni catalyst for C–H activation of heteroarene. The key to simultaneous C–H/C–O bond activation is the use of sterically demanding o-tolylMgBr. The protocol is effective for a wide scope of substrates including naphthyl methyl ethers, anisoles, and a variety of other heteroarene derivatives. Detailed mechanistic
Catalytic Oxidative Coupling of Primary Amines under Air: A Flexible Route to Benzimidazole Derivatives
作者:Khac Minh Huy Nguyen、Martine Largeron
DOI:10.1002/ejoc.201501520
日期:2016.2
inspired by copper amineoxidases, we disclose herein the scope and factors influencing the success of the cooperative action of CuBr2 as electron-transfer mediator and a topaquinone-like substrate-selective catalyst in the oxidative cyclocondensation of primary amines with o-aminoanilines. This one-pot atom-economic multistep process, which works under green conditions with ambient air as the terminal
“Dance reaction” on the aromatic ring is a powerful method in organic chemistry to translocate functional groups on arene scaffolds. Notably, dance reactions of halides and pseudohalides offer a unique platform for the divergent synthesis of substituted (hetero)aromatic compounds when combined with transition-metal-catalyzed coupling reactions. Herein, we report a tandemreaction of ester dance and
the strongest synthetic C–H hydride donors; however, its reductive regeneration requires highly reducing conditions. In this study, we synthesized various oxidized and reducedforms of BIH derivatives with aryl groups at the 2-position and investigated their photophysical and electrochemical properties. 4-(Dimethylamino)phenyl-substituted BIH exhibited salient red-shifted absorption compared with other