107553-43-5Relevant articles and documents
Regioselective synthesis of fused imidazo[1,2- a ]pyrimidines via intramolecular C-N bond formation/6- endo-dig cycloisomerization
Kumar, Atul,Kumar, Mukesh,Maurya, Shivam,Khanna, Ranjana S.
, p. 6905 - 6912 (2014)
An efficient regioselective cascade synthesis of N-fused imidazo heterocycles has been developed. This cascade transformation proceeds via a transition-metal (copper/silver) catalyzed coupling reaction between 2-aminobenzimidazole, aldehydes, and alkynes leading to the formation of propargylamine intermediate, which regioselectively undergoes 6-endo-dig cyclization through intramolecular N-H bond activation interceded C-N bond formation leading to highly functionalized imidazo[1,2-a]pyrimidines in good to excellent yields.
One-pot synthesis of highly functionalized pyrimido[1,2-b]indazoles via 6-endo-dig cyclization
Palaniraja, Jeyakannu,Roopan, Selvaraj Mohana,Rayalu, G. Mokesh
, p. 24610 - 24616 (2016)
An efficient synthesis of nitrogen ring junction pyrimido-indazoles has been developed. This is a metal catalyzed transformation that proceeds via A3 coupling reaction between 1H-indazol-3-amine, aromatic aldehydes and alkynes, which undergoes
Copper oxide nanoparticle catalysed synthesis of imidazo[1,2-a]pyrimidine derivatives, their optical properties and selective fluorescent sensor towards zinc ion
Rawat, Manish,Rawat, Diwan S.
supporting information, p. 2341 - 2346 (2018/05/23)
Synthesis of biologically active fused imidazo[1,2-a]pyrimidines were achieved via A3 coupling involving 2-aminobenzimidazole, aldehyde and terminal alkyne, followed by 6-endo-dig cyclization using copper oxide nanoparticles under solvent free