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1,2,3‐Triazole derivatives of 3‐ferrocenylidene‐2‐oxindole: Synthesis, characterization, electrochemical and antimicrobial evaluation
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Citations
50
References
2019
Year
Derivative (Chemistry)Bioorganic ChemistryDerivativesNatural SciencesAntimicrobial EvaluationChemical DerivativeOrganic ChemistryAntimicrobial CompoundChemistryHeterocycle ChemistryTriazole‐linked BenzylPharmacologyAliphatic ConjugatesPharmaceutical ChemistrySynthetic ChemistryCorresponding Conjugates
A series of bioactive, triazole‐linked benzyl, aryl, sugar and aliphatic conjugates of 3‐ferrocenylidene‐oxindole have been synthesized. A facile 1,3‐dipolar‐Huisgen coupling reaction of the respective azides with the 3‐ferrocenylidene‐oxindole N‐propargyl moiety ( 3 ) gave the corresponding conjugates ( 5a–n ). All the newly synthesized compounds ( 5a–n ) were characterized by 1 H‐NMR, 13 C‐NMR, HRMS, Fourier transform‐infrared spectroscopy and elemental analysis. The UV–Vis and electrochemical studies of these compounds were performed in dimethylsulfoxide solutions. The structure of compound ( 3 ) was determined by single crystal X‐ray diffraction study. These compounds exhibited moderate to good antimicrobial activity against Gram‐positive and Gram‐negative strains.
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