2021
DOI: 10.1007/s12633-021-00942-7
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Preparation of Core/Shell CaO@SiO2-SO3H as a Novel and Recyclable Nanocatalyst for One-Pot Synthesize of Dihydropyrano[2,3-c]Pyrazoles and Tetrahydrobenzo[b]Pyrans

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Cited by 16 publications
(16 citation statements)
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“…A new acid catalyst, CaO@SiO 2 ‐SO 3 H, was developed by Sameri et al [ 94 ] for the synthesis of tetrahydrobenzopyrans and dihydropyrano[2,3‐c]pyrazoles. The catalyst was prepared by stabilizing of sulfonic acid on the surface of SiO 2 ‐coated CaO NPs and was well characterized by several techniques, namely, Fourier transform‐infrared (FT‐IR), X‐ray diffraction analysis (XRD), field emission scanning electron microscope (FE‐SEM), energy dispersive X‐ray spectroscopy (EDS), wavelength dispersive X‐ray analysis (WDX), and thermogravimetric analysis (TGA).…”
Section: Different Synthetic Methodologies For Substituted Pyran Deri...mentioning
confidence: 99%
“…A new acid catalyst, CaO@SiO 2 ‐SO 3 H, was developed by Sameri et al [ 94 ] for the synthesis of tetrahydrobenzopyrans and dihydropyrano[2,3‐c]pyrazoles. The catalyst was prepared by stabilizing of sulfonic acid on the surface of SiO 2 ‐coated CaO NPs and was well characterized by several techniques, namely, Fourier transform‐infrared (FT‐IR), X‐ray diffraction analysis (XRD), field emission scanning electron microscope (FE‐SEM), energy dispersive X‐ray spectroscopy (EDS), wavelength dispersive X‐ray analysis (WDX), and thermogravimetric analysis (TGA).…”
Section: Different Synthetic Methodologies For Substituted Pyran Deri...mentioning
confidence: 99%
“…[ 24 ] Silica‐coated CaO nanoparticles were prepared by the Stober method. [ 22 ] Briefly, nano‐CaO (1 g) was sonicated in a mixture of ethanol (40 ml), deionized water (6 ml), and 1.5 ml of 25 wt% concentrated aqueous ammonia for 20 min at room temperature. Then, 1.4 ml of tetraethyl orthosilicate (TEOS) was added and the resulting mixture stirred for 22 h at room temperature under N 2 atmosphere.…”
Section: Methodsmentioning
confidence: 99%
“…( C) M.P (Lit.) ( C) [38] 22 3-OEt-4-OHC 6 H 3 7 h 20 95 187-189 186-190 [37] 23 2-naphthaldehyde 7i 25 90 196-197 205-207 [41] 24 terephthalaldehyde 7j 40 85 235-237 236-238 [42] 25 [ [22] 30 1-naphthaldehyde 8e 20 93 213-215 214-215 [45] 31 Pyridine-4-carbaldehyde 8f 20 95 260-262 265-266 [46] 32 2,2 0 -(butane-1,4-diylbis (oxy) dibenzaldehyde 8 g 25 95 209-211 209-211 [22] 33 [ comparable, suitable, and efficient catalyst for the synthesis of desired 4H-pyrans. The application of CaO@SiO 2 -NH 2 -Sal-Zn as a hybrid catalyst in solvent-free medium at room temperature led to the greener condition for this synthetic protocol.…”
Section: Preparation and Characterization Of Cao@sio 2 -Nh 2 -Sal-zn ...mentioning
confidence: 99%
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“…Moreover, for the synthesis of benzo [4,5]imidazo[1,2-a]pyrimidine derivatives at 110 C under solvent-free conditions, 95% yield was obtained. Signicantly, phthalazine-trione derivatives are well-known heterocycles used in the pharmaceutical and biological elds including vaso-relaxants, 190 antifungal, 191 antimicrobial, 192 anti-cancer, 193 and anti-inammatory agents. 194 Besides, benzo [4,5]imidazo [1,2-a]pyrimidines are biologically related fused pyrimidine derivatives, which demonstrate highlighted therapeutic and biological characteristics such as antimicrobial, 195 anti-inammatory, 196 protein kinase inhibitor, 197 and anticancer.…”
Section: Application Of Micro and Nanoscale Magnetic Catalytic System...mentioning
confidence: 99%