A series of 1H-1,2,3-triazoles 12a–g and 13a–g having 4H-pyrano[2,3-d]pyrimidine and D-glucose rings was synthesized by click chemistry and their inhibitory activity against UDP-N-acetylglucosamine enolpyruvyl transferases (MurA & MurZ) was examined.
The present review article focuses on recent advances in the nanocatalyzed multicomponent synthesis of hybrid molecules with structural diversity incorporating medicinally privileged heterocyclic substructures.
Starch as catalyst for organic reactions.
A novel magnetic resorcinol–formaldehyde-supported isatin-Schiff-base/Fe complex (Fe3O4@RF-ISB/Fe) is prepared, characterized and used as a powerful and highly recoverable nanocatalyst in the synthesis of pyrano[2,3-d]pyrimidines.
The past decade has witnessed significant progress in synthesizing structurally diverse and biologically relevant pyrano[2,3-c]pyrazole derivatives through the integration of green methodologies.