205655-12-5Relevant articles and documents
Gold-catalyzed redox synthesis of imidazo[1,2-a]pyridines using pyridine N-oxide and alkynes
Talbot, Eric P. A.,Richardson, Melodie,McKenna, Jeffrey M.,Toste, F. Dean
, p. 687 - 691 (2014)
A mild, catalytic, atom economical synthesis of imidazo[1,2-a]pyridines has been developed: catalytic dichloro(2-pyridinecarboxylato)gold [PicAuCl 2] in the presence of an acid produces a range of imidazo[1,2-a]pyridines in good yields starting
Iodine mediated oxidative cross coupling of 2-aminopyridine and aromatic terminal alkyne: A practical route to imidazo[1,2-: A] pyridine derivatives
Samanta, Surya Kanta,Bera, Mrinal K.
, p. 6441 - 6449 (2019/07/10)
A novel, transition-metal free route leading to imidazo[1,2-a]pyridine derivatives via iodine mediated oxidative coupling between 2-aminopyridine and aromatic terminal alkyne has been demonstrated. This newly developed method discloses an operationally simple way for the construction of imidazoheterocycles. Commercially available antiulcer drug zolimidine may readily be synthesized employing this method.
Potential inhibitors of plasmodial heme oxygenase; an innovative approach for combating chloroquine resistant malaria
Srivastava, Pratima,Pandey, Vikash Chandra,Misra, Anju Prabha,Gupta, Preeti,Raj, Kanwal,Bhaduri, Amiya Prasad
, p. 181 - 187 (2007/10/03)
Syntheses of imidazo-pyridines and substituted prolines and their effect on heme oxygenase activity of Plasmodium yoelii and corresponding infected host have been studied. Six compounds in vitro and one in vivo showed selective inhibition of parasite enzy
