1334500-68-3Relevant articles and documents
Copper-catalyzed C-N bond formation using dialkyl azodicarboxylate as the amination reagent
Samzadeh-Kermani, Alireza
, p. 463 - 465 (2016/01/12)
An efficient copper-catalyzed reaction for C-N bond formation using aryl halides, dialkyl azodicarboxylate, and a hydride source is reported. Using this procedure, aryl iodides reacted at ambient conditions, while aryl bromides required heating to 60 °C to accomplish the transformation. Various functional groups were tolerated under the optimum conditions.
Sodium hydride induced N-arylation of diisopropyl azodicarboxylate by aryl trifluoromethanesulfonates
Yavari, Issa,Ghazanfarpour-Darjani, Majid,Bayat, Mohammad J.,Malekafzali, Alaleh
, p. 942 - 944 (2015/04/27)
A method for intermolecular N-arylation of the anionic species derived from diisopropyl azodicarboxylate and sodium hydride by aryl trifluoromethanesulfonates, in the presence of a ligand-free copper(I) oxide catalyst at 80 °C in N,N-dimethylformamide, is reported. A variety of functionalized aryl triflouromethanesulfonates were efficiently coupled by this method.