1398412-30-0Relevant academic research and scientific papers
Iron-catalyzed C-N bond formation via oxidative Csp3-H bond functionalization adjacent to nitrogen in amides and anilines: Synthesis of N-alkyl and N-benzyl azoles
Saidulu,Kumar, R. Arun,Reddy, K. Rajender
, p. 4200 - 4203 (2015)
Iron catalyzed oxidative protocol was developed to couple azoles with amides to generate N-alkylazole derivatives in moderate to excellent yields using tertiarybutyl hydroperoxide as an oxidant under mild reaction conditions. Furthermore, this protocol ex
Iron Nanoparticles Embedded in Graphitic Carbon Matrix as Heterogeneous Catalysts for the Oxidative C?N Coupling of Aromatic N?H Compounds and Amides
He, Jinbao,Dhakshinamoorthy, Amarajothi,Primo, Ana,Garcia, Hermenegildo
, p. 3003 - 3012 (2017)
Fe or Co nanoparticles (NPs) and two nanoparticulate Fe-Co alloys having different Fe/Co atomic ratio with average particle size ranging from 10.9 to 26.5 nm embedded in turbostratic graphitic carbon matrix have been prepared by pyrolysis at 900 °C under
A Metal-Free Cross-Dehydrogenative Coupling Reaction of Amides to Access N -Alkylazoles
Zhu, Zheng,Wang, Yufeng,Yang, Mingmeng,Huang, Ling,Gong, Jiuhan,Guo, Shengmei,Cai, Hu
, p. 2705 - 2708 (2016)
An iodine-catalyzed cross-dehydrogenative coupling reaction of N-alkyl amides and azoles is reported. The catalytic system provides an efficient method for introducing amides onto azoles, especially onto benzotriazoles.
Iron-catalyzed N-alkylation of azoles via cleavage of an sp3 C-H bond adjacent to a nitrogen atom
Xia, Qinqin,Chen, Wanzhi
supporting information, p. 9366 - 9373,8 (2012/12/12)
Iron-catalyzed direct C-N bond formation between azoles and amides is described. The oxidative coupling reactions of sp3 C-H bonds adjacent to a nitrogen atom in amides and sulfonamides with the N-H bond in azoles proceeded smoothly in the presence of FeCl2 and di-tert-butyl peroxide (DTBP).
