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dc.contributor.authorBiradar, J S-
dc.contributor.authorRajesab, P-
dc.contributor.authorSasidhar, B S-
dc.date.accessioned2014-05-26T09:44:18Z-
dc.date.available2014-05-26T09:44:18Z-
dc.date.issued2014-
dc.identifier.citationJournal of Chemistry:Article ID 579612; 2014en_US
dc.identifier.issn2090-9063-
dc.identifier.urihttp://ir.niist.res.in:8080/jspui/handle/123456789/1460-
dc.description.abstractWe describe herein the design, synthesis, and pharmacological evaluation of novel series of imidazolopyridinyl indole analogues as potent antioxidants and antimicrobials. These novel compounds (3a-i) were synthesized by reacting 3,5-disubstituted-indole-2-carboxylic acid (1a-i) with 2,3-diamino pyridine (2) in excellent yield. The novel products were confirmed by their IR, H-1 NMR, C-13 NMR, mass spectral, and analytical data. These compounds were screened for their antioxidant and antimicrobial activities. Among the compounds tested, 3a-d showed the highest total antioxidant capacity, scavenging, and antimicrobial activities. Compounds 3c-d and 3g-h have shown excellent ferric reducing activity.en_US
dc.language.isoenen_US
dc.publisherHindawi Publishing Corporationen_US
dc.subjectImidazolopyridinyl indolesen_US
dc.subjectAntioxidantsen_US
dc.subjectAntimicrobialsen_US
dc.titleMicrowave assisted synthesis of novel imidazolopyridinyl indoles as potent antioxidant and antimicrobial agentsen_US
dc.typeArticleen_US
Appears in Collections:2014

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