“…Sajjadi et al (2023), for instance, reported on the synthesis of dihydropyrano[2,3c]pyrazoles via Knoevenagel-Michael multiple reactions by using green catalyst Fe 3 O 4 @gC 3 N 4 for the reaction of aldehydes, phenylhydrazine, ethyl acetoacetate and malononitrile under 1 h reflux to achieve 97 % yield of product (Route 1). [51] This reaction has also been reported by using numerous catalysts such as 1,8-diazabicyclo[5.4.0]-undec-7-en-8-ium acetate ([DBU][Ac], [59] HMS/PrÀ Rh-Zr, [60] H 3 PO 4 /Al 2 O 3 , P 2 O 5 /SiO 2 , starch sulfuric acid, cellulose sulfuric acid, [61] thiourea dioxide (TUD), [62] PVCÀ EDAÀ CeIII, [63] citrus limon (lemon juice), [64] agave leaf ash extract, [65] piperidine, [66] sodium lactate, [67] NiWO 4 , [68] PBCMOamine, [69] CaO nanoparticles, [70] Fe 3 O 4 @chitosan-tannic acid bionanocomposite, [71] FSiPSS nano-catalyst, [72] nano ZrO 2 , [73] lactic acid : urea : NH 4 Cl, [74] H 4 [SiW 12 O 40 ], [75] NiFe 2 O 4 @SiO 2 À H 3 PW 12 O 40 (NFSÀ PWA), [76] Fe 3 O 4 @SiO 2 @CoSB, [77] PAN@melamine/Fe 3 O 4 nanocomposite, [78] isonicotinic acid, [79] nano-[Fe-PSMP]Cl 2 , [80] Fe 3 O 4 /MIP-202-H 4 WO 5 , [81] Zn(L-proline) 2 , [82] baker's yeast, [83] solar radiation, [84] Cu-DABP@Fe 3 O 4 /MCM-41, [85] Fe 3 O 4 @NFC@Co(II), [86] PdO/Al-SBA-15, [87] (MnCoFe 2 O 4 @Niacin-SO 3 H) + Cl À , [88] Zn-CA-MOFs [89] and Na 2 CaP 2 O 7 . [90] In 2022, Nguyen and coworkers reported different routes to the synthesis of pyrano[2,3-c]pyrazole derivatives, which involved a four-component reaction of benzyl alcohols, phenylhydrazine, ethyl acetoacetate and malononitrile with the aid of sulfonated amorphous carbon and eosin Y as c...…”