Method for the synthesis of chromenopyrimidine-fused azoles by copper-catalyzed intramolecular hetero-Diels–Alder reaction

Identificador:  imarina:9322141

Handle: https://hdl.handle.net/20.500.11797/imarina9322141

Autores:  Ghomi MK; Alizadeh N; Moazzam A; Hosseini S; Bahadorikhalili S; Larijani B; Mahdavi M

Resumen:
[Figure not available: see fulltext.] One-pot efficient copper-catalyzed approach for the synthesis of tetracyclic chromeno[4',3':4,5]pyrimido[1,2-b]indazolone and chromeno[4,3-d]-[1,2,4]triazolo[4,3-a]pyrimidine derivatives as a class of pharmacologically interesting compounds through the intramolecular domino condensation–aza-Diels–Alder reaction of aminoazoles and o-propargylated salicylaldehydes under reflux conditions has been described.