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Efficient Sonogashira and A<sup>3</sup> coupling reactions catalyzed by biosynthesized magnetic Fe<sub>3</sub>O<sub>4</sub>@Ni nanoparticles from <scp><i>Euphorbia maculata</i></scp> extract
36
Citations
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References
2020
Year
Chemical EngineeringCatalytic ApplicationEngineeringIndustrial CatalysisEfficient SonogashiraNatural SciencesDiversity-oriented SynthesisBiochemical EngineeringBioorganometallic ChemistryNanocatalysisCatalysisMolecular CatalysisChemistryO 4Catalyst PreparationFe 3Reaction TimesCatalytic Synthesis
In this work, biosynthesized Fe 3 O 4 @Ni nanoparticles using Euphorbia maculata aqueous have been used as effective catalysts in the synthesis of 2,3‐disubstituted benzo[ b ]furan derivatives using three component coupling of aldehydes, secondary amines and alkynes (A 3 coupling reaction). Using novel nanoscale materials, the current green, practical and economical method leads to short reaction times and high yields. The biosynthesized catalyst was also successfully employed in the Sonogashira cross‐coupling reactions of various aryl halides with phenylacetylene. The best performance was observed using just 20 mg of the catalyst and ethanol as a green solvent. The developed protocol provides easy workup, short reaction times and good to excellent product yields. Furthermore, since the composite is highly stable, an external permanent magnet can be easily used for separating the catalyst. Thus, the catalyst can be recycled several times without considerable loss of catalytic activity.
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