DC Field | Value | Language |
---|---|---|
dc.contributor.author | Patel, M. V. | - |
dc.contributor.author | Kaneriya, D. J. | - |
dc.date.accessioned | 2024-11-18T05:16:57Z | - |
dc.date.available | 2024-11-18T05:16:57Z | - |
dc.date.issued | 2024 | - |
dc.identifier.citation | Citation : Patel, M. V., & Kaneriya, D. J. SYNTHESIS OF 2-((5-2-METHYLIMIDAZO [1, 2-A] PYRIDINE-3-YL)-1, 3, 4-OXADIAZOL-2-YL) THIO)-N-PHENYLACETAMIDE DERIVATIVES AND THEIR BIOLOGICAL EVALUATION | en_US |
dc.identifier.issn | 0974-1496 | e-ISSN: 0976-0083 | - |
dc.identifier.uri | http://10.9.150.37:8080/dspace//handle/atmiyauni/1611 | - |
dc.description.abstract | In this work, a novel series of compounds based on 2-((5-(2-methylimidazo [1, 2-a] pyridine-3-yl)-1, 3, 4-oxadiazol-2-yl) thio)-N-phenylacetamide derivatives was meticulously synthesized and thoroughly characterized through infrared spectroscopy, 1H NMR, 13C NMR, and mass spectroscopies. The systematic synthesis and characterization of these compounds aimed to establish a foundation for investigating their potential antibacterial and antifungal activities. The research methodology involved a multi-faceted approach, wherein the synthesized compounds were subjected to rigorous testing to evaluate their effectiveness against bacterial and fungal strains. The experimental design included a range of concentrations to provide a comprehensive understanding of the compounds’ inhibitory effects. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Rasayan J. Chem | en_US |
dc.subject | SYNTHESIS | en_US |
dc.subject | N-PHENYLACETAMIDE | en_US |
dc.subject | DERIVATIVES | en_US |
dc.subject | THEIR BIOLOGICAL EVALUATION | en_US |
dc.title | SYNTHESIS OF 2-((5-2-METHYLIMIDAZO [1, 2-A] PYRIDINE-3-YL)-1, 3, 4-OXADIAZOL-2-YL) THIO)-N-PHENYLACETAMIDE DERIVATIVES AND THEIR BIOLOGICAL EVALUATION. | en_US |
dc.type | Article | en_US |
Appears in Collections: | 01. Journal Articles |
Files in This Item:
File | Description | Size | Format | |
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SYNTHESIS OF 2-((5-2-METHYLIMIDAZO[1,2-A]PYRIDINE-.pdf | 1.1 MB | Adobe PDF | View/Open |
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