Matches in SemOpenAlex for { <https://semopenalex.org/work/W4281915181> ?p ?o ?g. }
Showing items 1 to 91 of
91
with 100 items per page.
- W4281915181 endingPage "626" @default.
- W4281915181 startingPage "626" @default.
- W4281915181 abstract "Sulfonated polymer-based materials, among heterogeneous catalysts, are frequently utilized in chemical transformations due to their outstanding chemical and physical durability. In this regard, a magnetic sulfonated melamine–formaldehyde resin (MSMF) catalyst was successfully prepared from a mixture of sulfonated melamine–formaldehyde and Fe3O4 nanoparticles in two steps. MSMF was used as a heterogeneous catalyst for the one-pot, three-component condensation of benzyl pyrazolyl naphthoquinones in water as a green solvent and 4-[(indol-3-yl)-arylmethyl]-1-phenyl-3-methyl-5-pyrazolones. The antimicrobial and antioxidant activities of catalyst, benzyl pyrazolyl naphthoquinones, and 4-[(indol-3-yl)-arylmethyl]-1-phenyl-3-methyl-5-pyrazolones were evaluated using agar disk-diffusion and DPPH assays, respectively. The antioxidant activity of the catalyst and 4-[(indol-3-yl)-arylmethyl]-1-phenyl-3-methyl-5-pyrazolones was found to be 75% and 90%, respectively. Furthermore, catalyst, benzyl pyrazolyl naphthoquinones, and 4-[(indol-3-yl)-arylmethyl]-1-phenyl-3-methyl-5-pyrazolones exhibited antimicrobial activity against Staphylococcus aureus and Escherichia coli. In conclusion, MSMF is a superior catalyst for green chemical processes, owing to its high catalytic activity, stability, and reusability." @default.
- W4281915181 created "2022-06-13" @default.
- W4281915181 creator A5006302617 @default.
- W4281915181 creator A5043803511 @default.
- W4281915181 creator A5050146792 @default.
- W4281915181 creator A5073873928 @default.
- W4281915181 creator A5091863656 @default.
- W4281915181 date "2022-06-07" @default.
- W4281915181 modified "2023-09-30" @default.
- W4281915181 title "Magnetic Sulfonated Melamine-Formaldehyde Resin as an Efficient Catalyst for the Synthesis of Antioxidant and Antimicrobial Pyrazolone Derivatives" @default.
- W4281915181 cites W1485445093 @default.
- W4281915181 cites W1964056979 @default.
- W4281915181 cites W1969107619 @default.
- W4281915181 cites W1987394952 @default.
- W4281915181 cites W1989165468 @default.
- W4281915181 cites W1995355277 @default.
- W4281915181 cites W2003873084 @default.
- W4281915181 cites W2021524350 @default.
- W4281915181 cites W2024289681 @default.
- W4281915181 cites W2043277700 @default.
- W4281915181 cites W2054488432 @default.
- W4281915181 cites W2079071691 @default.
- W4281915181 cites W2079961827 @default.
- W4281915181 cites W2090033846 @default.
- W4281915181 cites W2095065286 @default.
- W4281915181 cites W2101130244 @default.
- W4281915181 cites W2109928760 @default.
- W4281915181 cites W2129410342 @default.
- W4281915181 cites W2136548451 @default.
- W4281915181 cites W2145992008 @default.
- W4281915181 cites W2161392734 @default.
- W4281915181 cites W2299819625 @default.
- W4281915181 cites W2536269321 @default.
- W4281915181 cites W2565301350 @default.
- W4281915181 cites W2950989864 @default.
- W4281915181 cites W2956417611 @default.
- W4281915181 cites W2970021180 @default.
- W4281915181 cites W2983006851 @default.
- W4281915181 cites W3003886191 @default.
- W4281915181 cites W3046952915 @default.
- W4281915181 cites W4220665473 @default.
- W4281915181 cites W4236999489 @default.
- W4281915181 doi "https://doi.org/10.3390/catal12060626" @default.
- W4281915181 hasPublicationYear "2022" @default.
- W4281915181 type Work @default.
- W4281915181 citedByCount "6" @default.
- W4281915181 countsByYear W42819151812022 @default.
- W4281915181 countsByYear W42819151812023 @default.
- W4281915181 crossrefType "journal-article" @default.
- W4281915181 hasAuthorship W4281915181A5006302617 @default.
- W4281915181 hasAuthorship W4281915181A5043803511 @default.
- W4281915181 hasAuthorship W4281915181A5050146792 @default.
- W4281915181 hasAuthorship W4281915181A5073873928 @default.
- W4281915181 hasAuthorship W4281915181A5091863656 @default.
- W4281915181 hasBestOaLocation W42819151811 @default.
- W4281915181 hasConcept C13965031 @default.
- W4281915181 hasConcept C161790260 @default.
- W4281915181 hasConcept C178790620 @default.
- W4281915181 hasConcept C185592680 @default.
- W4281915181 hasConcept C2775930285 @default.
- W4281915181 hasConcept C2778802955 @default.
- W4281915181 hasConcept C2908653458 @default.
- W4281915181 hasConcept C4937899 @default.
- W4281915181 hasConceptScore W4281915181C13965031 @default.
- W4281915181 hasConceptScore W4281915181C161790260 @default.
- W4281915181 hasConceptScore W4281915181C178790620 @default.
- W4281915181 hasConceptScore W4281915181C185592680 @default.
- W4281915181 hasConceptScore W4281915181C2775930285 @default.
- W4281915181 hasConceptScore W4281915181C2778802955 @default.
- W4281915181 hasConceptScore W4281915181C2908653458 @default.
- W4281915181 hasConceptScore W4281915181C4937899 @default.
- W4281915181 hasIssue "6" @default.
- W4281915181 hasLocation W42819151811 @default.
- W4281915181 hasOpenAccess W4281915181 @default.
- W4281915181 hasPrimaryLocation W42819151811 @default.
- W4281915181 hasRelatedWork W1553678874 @default.
- W4281915181 hasRelatedWork W1971127514 @default.
- W4281915181 hasRelatedWork W1972131152 @default.
- W4281915181 hasRelatedWork W1986974960 @default.
- W4281915181 hasRelatedWork W2483706346 @default.
- W4281915181 hasRelatedWork W2582719159 @default.
- W4281915181 hasRelatedWork W2930376949 @default.
- W4281915181 hasRelatedWork W4235265576 @default.
- W4281915181 hasRelatedWork W4285270666 @default.
- W4281915181 hasRelatedWork W1507804713 @default.
- W4281915181 hasVolume "12" @default.
- W4281915181 isParatext "false" @default.
- W4281915181 isRetracted "false" @default.
- W4281915181 workType "article" @default.