Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/2935
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dc.contributor.authorJanardhan, B.-
dc.contributor.authorVijayalaxmi, S-
dc.contributor.authorRajitha, B-
dc.date.accessioned2025-01-24T09:52:53Z-
dc.date.available2025-01-24T09:52:53Z-
dc.date.issued2013-
dc.identifier.citation10.1002/jhet.1564en_US
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/2935-
dc.descriptionNITWen_US
dc.description.abstractA novel series of poly-substituted pyridines (7-(substituted aryl)-3,11-dimethoxy-5,6,8,9-tetrahydro-dibenzo[c,h]acridines) were synthesized via one-pot multicomponent approach using sulfamic acid as a catalyst and evaluated for their antimicrobial activity. The results indicate that the poly-substituted series (4a, 4b, 4c, 4d, 4e, 4f, 4g, 4h, 4i) showed weak to moderate antibacterial activity. However, compound (4c) had shown good antifungal activity against Candida rugosa with standard antifungal drug Amphotericin-B. Analogue (4c) was considered to be a lead compound for subsequent standard optimization.en_US
dc.language.isoenen_US
dc.publisherJournal of Heterocyclic Chemistryen_US
dc.subjectSulfamic Acid-Catalyzeden_US
dc.subjectPoly-Substituted Pyridinesen_US
dc.titleSulfamic acid-catalyzed multicomponent one-pot synthesis of poly-substituted pyridines and their antimicrobial activityen_US
dc.typeArticleen_US
Appears in Collections:Chemistry



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