2014
DOI: 10.1016/j.tet.2014.03.024
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Synthesis of pyranopyrazoles using magnetic Fe3O4 nanoparticles as efficient and reusable catalyst

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Cited by 118 publications
(25 citation statements)
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“…Comparing the results, the optimum ones (high yield of product within shortest reaction time) were under solvent-free condition at 60°C (entry 2). Subsequently, the optimum amount of catalyst was found as 0.03 g. Also, the results for the reaction in the presence of Fe 3 O 4 , SiO 2 @Fe 3 O 4 and Fe 3 O 4 @SiO 2 -HMTA (entries [13][14][15] and also in the absence of the catalyst (entry 16) were not as good as the results obtained in the presence of Fe 3 O 4 @SiO 2 -HMTA-SO 3 H. Hence, to study the generality of the effect of Fe 3 O 4 @SiO 2 -HMTA-SO 3 H on this reaction, different pyranopyrazole derivatives (8a-m) were synthesized (Scheme 3), and the results are summarized in Table 2. It is observed that electron-donating substituents on phenyl ring make the reaction slower and lead to a lower yield of the corresponding products compared to electron-withdrawing substituents.…”
Section: Hmta-so 3 H Mnps In Synthesis Of Pyranopyrazole Derivativesmentioning
confidence: 99%
See 1 more Smart Citation
“…Comparing the results, the optimum ones (high yield of product within shortest reaction time) were under solvent-free condition at 60°C (entry 2). Subsequently, the optimum amount of catalyst was found as 0.03 g. Also, the results for the reaction in the presence of Fe 3 O 4 , SiO 2 @Fe 3 O 4 and Fe 3 O 4 @SiO 2 -HMTA (entries [13][14][15] and also in the absence of the catalyst (entry 16) were not as good as the results obtained in the presence of Fe 3 O 4 @SiO 2 -HMTA-SO 3 H. Hence, to study the generality of the effect of Fe 3 O 4 @SiO 2 -HMTA-SO 3 H on this reaction, different pyranopyrazole derivatives (8a-m) were synthesized (Scheme 3), and the results are summarized in Table 2. It is observed that electron-donating substituents on phenyl ring make the reaction slower and lead to a lower yield of the corresponding products compared to electron-withdrawing substituents.…”
Section: Hmta-so 3 H Mnps In Synthesis Of Pyranopyrazole Derivativesmentioning
confidence: 99%
“…[7] Thus, they can act as UV absorbers. Until now, various catalysts have been applied in the synthesis of pyranopyrazole derivatives, such as SBA-15-based catalysts, [8,9] L-proline, [10,11] ionic liquids, [12] magnetic nanoparticles (MNPs) [13] and ZrO 2 nanoparticles. [14] Due to the increasing consideration for the use of nanomagnetic catalysts in organic syntheses, [15][16][17][18] efforts have been made to modify the surface of MNPs for increasing their catalytic efficiency.…”
mentioning
confidence: 99%
“…Recently, several amendments have been done for the synthesis of dihydropyrano[2,3-c] pyrazole which involve the use of morpholine triflate [23], β-cyclodextrin [24], meglumine [25], L-proline [26], Fe 3 O 4 nanoparticles [27], green cellulose-based nanocomposite catalyst [28], lactic acid [29], isonicotinic acid [30], sodium dodecyl sulfate [31], molecular sieve [32], DABCO [33], lipase [34], bovine serum albumin [35], deep eutectic solvent [36], Ag/TiO 2 nano-thin films [37], Ba(OH) 2 [38], polyphosphoric acid supported nanoparticles [39], [Yb(OTf) 3 ] ytterbium triflate [40], and micellar medium [41].…”
Section: Introductionmentioning
confidence: 99%
“…Also, various methods are applied for the synthesis, and stabilization of such magnetic nanoparticles (NPs) [5][6][7][8][9][10]. Encapsulation with silica is a one of the important method for stabilization and changing surface reactivity [11][12][13].…”
Section: Introductionmentioning
confidence: 99%