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. 2026 Jan 28;8(5):1585–1597. doi: 10.1039/d5na01102g

Table 4. Comparison of the synthesis of compounds 6a, 7a and 8a using the Arg@ZY-Fe3O4 catalyst with other reported methods.

Product Catalyst Conditions Time (min) Yield (%)
6a K2CO3 (1 mmol) MDWa, 70 °C 240 96 (ref. 46)
6a Zn(l-proline)2 (20 mol%) EtOH/H2O, reflux 240 89 (ref. 55)
6a Nano-cellulose-OTiCl3 (3 mg) EtOH, reflux 20 94 (ref. 52)
6a Triethanolamine (30 mol%) H2O, reflux 45 92 (ref. 53)
6a Arg@ZY-Fe3O4 (10 wt%) H2O, 90 °C 5 97 (this work)
7a Picolinic acid (15 mol%) EtOH/H2O, 60 °C 10 98 (ref. 54)
7a Piperazine-GO (1 mol%) EtOH/H2O, 50 °C 15 95 (ref. 61)
7a Na3[CrMo6O24H6]·8H2O@ZrO2 (20 mg) EtOH, reflux 10 98 (ref. 44)
7a Talc (0.06 g) Solvent-free, 90 °C 35 90 (ref. 60)
7a Arg@ZY-Fe3O4 (10 wt%) H2O, 90 °C 7 95 (this work)
8a Talc (0.06 g) Solvent-free, 90 °C 40 91 (ref. 60)
8a Piperidine (0.5 mL) MW, 140 °C 2 87 (ref. 62)
8a Zn(l-proline)2 (20 mol%) EtOH/H2O, reflux 240 90 (ref. 55)
8a Piperazine-GO (3 mol%) Solvent-free, 100 °C 40 97 (ref. 61)
8a Arg@ZY-Fe3O4 (10 wt%) H2O, 90 °C 12 90 (this work)
a

Magnetized distilled water.