1198306-60-3Relevant academic research and scientific papers
Palladium-catalyzed oxidative intramolecular C-C bond formation via double sp2 C-H activation between the 2-position of imidazoles and a benzene ring
Sun, Manman,Wu, Huandong,Zheng, Junnan,Bao, Weiliang
supporting information; experimental part, p. 835 - 838 (2012/05/20)
Oxidative intramolecular C-C bond formation via double sp2 C-H activation between the 2-position of imidazoles and a benzene ring catalyzed by palladium(II) has been developed, which provides an atom-economical, concise and efficient methodology to synthesize imidazole- or benzimidazole-fused isoquinoline polyheteroaromatic compounds. Copyright
Iron-catalyzed cross-coupling reaction of vinyl bromides or chlorides with imidazoles in the absence of ligands and additives
Mao, Jincheng,Xie, Guanlei,Zhan, Jiaming,Hua, Qiongqiong,Shi, Daqing
experimental part, p. 1268 - 1272 (2009/12/30)
Highly effective coupling of imidazoles with (E)-vinyl halides can be achieved by using readily available iron catalysts under ligand-free, copper-free and palladium-free conditions. Coupling of (E)-vinyl bromides led to (Z)-products predominantly, while
