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dc.contributor.authorKalluraya, Balakrishna-
dc.contributor.authorGururaja, R.-
dc.contributor.authorRai, Ganesha-
dc.date.accessioned2013-10-04T10:42:40Z-
dc.date.available2013-10-04T10:42:40Z-
dc.date.issued2003-01-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/21501-
dc.description211-214en_US
dc.description.abstractReaction of 6-substituted-2-chloro-3-formylquinoline 1 and 3-substituted-4-amino-5-mercapto-1,2,4-triazole 2 gave the novel thiadiazepine derivatives 5 rather than expected Schiff bases 4. Alternatively, compounds 5 were also prepared by the reaction of 2 with 6-substitutcri quinolones 3. The structures of the newly synthesized compounds have been proposed on the basis of elemental analysis, IR,1H NMR and mass spectral data. Some of the new synthetic compounds were also screened for their antibacterial and antifungal activity. Most of them showed significant activity.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-B Vol.42B(01) [January 2003]en_US
dc.titleOne pot reaction: Synthesis, characterization and biological activity of 3-alkyl/aryl-9- substituted 1,2,4-triazolo[3,4-b] [1,3,4]quinolinothiadiazepinesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.42B(01) [January 2003]

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