110-125One-pot multi-component synthesis of tri and tetra-substituted coumarin-imidazole conjugates have been achieved in good to excellent yield under conventional and microwave methods in optimized catalyst condition. Further, they have been evaluated for antimicrobial activity against Gram positive Bacillus flexus and Gram negative Pseudomonas Spp. bacterial strains and two strains of fungi Scopulariopsis spp. and Aspergillus tereus organisms. The results of microbial activity are promising against tested organisms. The molecular docking study has been performed for all the compounds and docking scores are excellent. Synthesized compounds have been characterized by IR, NMR, mass and a few of them by single crystal X-ray analysis
Introduction: Nowadays, researchers are progressively concentrated to generate economical, affordabl...
<div><p>The control of antimicrobial resistance (AMR) seems to have come to a dead end. The major co...
AbstractA novel series of 2-[5-(4-substituted phenyl)furan-2-yl]-4,5-diphenyl-1H-imidazole derivativ...
159-173The green chemistry approach provides for the synthesis of coumarin-1,4-dihydropyridine scaff...
The green chemistry approach provides for the synthesis of coumarin-1,4-dihydropyridine scaffolds 6a...
A series of new conjugated compounds with a -SCH₂- linkage were synthesized by chemical methods from...
The overuse and lack of regulation of antibiotics has resulted in the emergence of antibiotic�resist...
The overuse and lack of regulation of antibiotics has resulted in the emergence of antibiotic�resist...
The overuse and lack of regulation of antibiotics has resulted in the emergence of antibiotic�resist...
AbstractIn modern drug designing, molecular docking is routinely used for understanding drug-recepto...
Introduction: Nowadays, researchers are progressively concentrated to generate economical, affordabl...
AbstractAs part of our exploration for new antifungal agents, substituted 4,5-diphenyl imidazolyl py...
166-173Pechmann reaction is mainly used for the synthesis of substituted coumarins as it can be exec...
Introduction: Nowadays, researchers are progressively concentrated to generate economical, affordabl...
Four 4-hydroxycoumarin derivatives were synthesized and the structure was confirmed by NMR spectrosc...
Introduction: Nowadays, researchers are progressively concentrated to generate economical, affordabl...
<div><p>The control of antimicrobial resistance (AMR) seems to have come to a dead end. The major co...
AbstractA novel series of 2-[5-(4-substituted phenyl)furan-2-yl]-4,5-diphenyl-1H-imidazole derivativ...
159-173The green chemistry approach provides for the synthesis of coumarin-1,4-dihydropyridine scaff...
The green chemistry approach provides for the synthesis of coumarin-1,4-dihydropyridine scaffolds 6a...
A series of new conjugated compounds with a -SCH₂- linkage were synthesized by chemical methods from...
The overuse and lack of regulation of antibiotics has resulted in the emergence of antibiotic�resist...
The overuse and lack of regulation of antibiotics has resulted in the emergence of antibiotic�resist...
The overuse and lack of regulation of antibiotics has resulted in the emergence of antibiotic�resist...
AbstractIn modern drug designing, molecular docking is routinely used for understanding drug-recepto...
Introduction: Nowadays, researchers are progressively concentrated to generate economical, affordabl...
AbstractAs part of our exploration for new antifungal agents, substituted 4,5-diphenyl imidazolyl py...
166-173Pechmann reaction is mainly used for the synthesis of substituted coumarins as it can be exec...
Introduction: Nowadays, researchers are progressively concentrated to generate economical, affordabl...
Four 4-hydroxycoumarin derivatives were synthesized and the structure was confirmed by NMR spectrosc...
Introduction: Nowadays, researchers are progressively concentrated to generate economical, affordabl...
<div><p>The control of antimicrobial resistance (AMR) seems to have come to a dead end. The major co...
AbstractA novel series of 2-[5-(4-substituted phenyl)furan-2-yl]-4,5-diphenyl-1H-imidazole derivativ...