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http://nopr.niscpr.res.in/handle/123456789/60725Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Marri, Srinivas | - |
| dc.date.accessioned | 2022-10-21T05:57:27Z | - |
| dc.date.available | 2022-10-21T05:57:27Z | - |
| dc.date.issued | 2022-10 | - |
| dc.identifier.issn | 2583-1321 (Online); 0019-5103 (Print) | - |
| dc.identifier.uri | http://nopr.niscpr.res.in/handle/123456789/60725 | - |
| dc.description | 1046-1053 | en_US |
| dc.description.abstract | Synthesis of novel 5-methyl-1-(4-(6-methylimidazo[1,2-b]isoxazol-3-yl)phenyl)-3-aryl-1,3,5-triazinane-2-thiones 6 has been achieved by the reaction of 3-amino-5-methylisoxazole 1 with p-nitrophenacyl bromide, followed by reduction of 3 with stannous chloride. Compounds 4 on treatment with different aryl isothiocyanates in refluxing benzene, followed by trimolecular condensation with 30% HCHO and methyl amine in ethanol affords the title compounds 6. The newly synthesized compounds 6 have been evaluated for their in vitro antimicrobial activity. Compounds 6 exhibit potent antimicrobial activity compared to that of standard drugs. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | NIScPR-CSIR,India | en_US |
| dc.source | IJC Vol.61(10) [Oct 2022] | en_US |
| dc.subject | 6-Methyl-3-arylimidazolo[1,2-b]isoxazoles | en_US |
| dc.subject | 1,3,5-Triazinane-2-thiones | en_US |
| dc.subject | Trimolecular condensation | en_US |
| dc.subject | Antibacterial activity | en_US |
| dc.subject | Antifungal activity | en_US |
| dc.title | Synthesis and antimicrobial activity of novel 5-methyl-1-(4-(6-methylimidazo [1,2-b]isoxazol-3-yl)phenyl)-3-aryl-1,3,5-triazinane-2-thiones | en_US |
| dc.type | Article | en_US |
| dc.identifier.doi | https://doi.org/10.56042/ijc.v61i10.62377 | en_US |
| Appears in Collections: | IJC Vol.61(10) [Oct 2022] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJC 61(10) 1046-1053.pdf | 3.11 MB | Adobe PDF | View/Open |
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