“…The synthesis of pyran derivatives has garnered widespread attention among researchers owing to their signi cance, prompting exploration through various methodologies, including microwave [33] and ultrasound irradiation in water [17,26,34] as well as the use of different catalysts under various conditions such as: halide ions [35][36], ionic liquids [37][38][39], triethylamine (NEt 3 ) [26], sophisticated organocatalysts potassium-N-oxyl phthalimide [40], heterogeneous catalysts [41], alkalin metallo-organic ([Mg 3 (NDC) 3 (DMF) 4 ]-H 2 O) [42], magnetic nanoparticles [43], polyethylene glycol (PEG) [44], piperidine [45], NaOH in water [46], 1,8-diazabicyclo [5. 4.0] undec-7-ene (DBU) in water [47], LiBr in water [48], sodium acetate combined with microwave irradiation [33], and CaO/KOH under solvent-free conditions [49]. However, while these methods exhibit varying degrees of success, they also present drawbacks such as elevated temperatures, moderate yields, limited applicability, prolonged reaction times, and reliance on harmful or costly solvents or catalysts.…”