1115604-53-9Relevant academic research and scientific papers
Influence of the 2-aryl group on the ipso electrophilic substitution process of 2-arylimidazo[1,2-a]pyridines
Salgado-Zamora, Hector,Velazquez, Manuel,Mejia, Daniel,Campos-Aldrete,Jimenez, Rogelio,Cervantes, Humberto
, p. 27 - 32 (2008)
A systematic study of electrophilic substitution reactions of 3-nitroso-2-arylimidazo[1,2-a]pyridine confirmed that the nitroso group may be ipso-substituted by bromine (NBS in DMF) and that bromine in turn may be substituted by the nitroso group. Electro
NaNO2/I2-Mediated Regioselective Synthesis of Nitrosoimidazoheterocycles from Acetophenones by a Domino Process
Mukhopadhyay, Sushobhan,Dighe, Shashikant U.,Kolle, Shivalinga,Shukla, Praveen K.,Batra, Sanjay
, p. 3836 - 3844 (2016)
A regioselective synthesis of nitrosoimidazoheterocycles from the reaction of 2-aminopyridines and acetophenones in the presence of NaNO2and I2is described. The reaction is suggested to proceed by a domino process involving sequentia
Regioselective synthesis of nitrosoimidazoheterocycles using tert-butyl nitrite
Monir, Kamarul,Ghosh, Monoranjan,Jana, Sourav,Mondal, Pallab,Majee, Adinath,Hajra, Alakananda
, p. 8717 - 8722 (2015/08/24)
A simple and practical method has been developed for the regioselective nitrosylation of imidazopyridines via C(sp2)-H bond functionalization using tert-butyl nitrite under mild reaction conditions in a short time. A library of 3-nitrosoimidazo
