1334500-70-7Relevant articles and documents
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)
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.
Cross-coupling reaction of aryl diazonium salts with azodicarboxylate using FeCl2
Khalaj,Ghazanfarpour-Darjani
, p. 80698 - 80701 (2015/10/06)
Arene diazonium salts have been employed as the aryl source in reaction with dialkyl azodicarboxylates to form N-aryl hydrazide derivatives. The optimum conditions are developed using FeCl2 in DMSO at 25 °C for 2 h. Various functional groups we