Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/21873
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dc.contributor.authorMohan, Jag-
dc.contributor.authorAnupama-
dc.date.accessioned2013-10-11T05:53:33Z-
dc.date.available2013-10-11T05:53:33Z-
dc.date.issued2002-03-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/21873-
dc.description628-630en_US
dc.description.abstract2, 3-Dihydro-6-ethyl-5H-as-triazino[5, 6-b]indole-3-thione 4 on condensation with α-haloketone gives 3-aroylmethylthio-6-ethyl-5H-as-triazino[5, 6-b]indolehydrobromide 5 which on PPA catalyzed cyclization furnishes 3-aryl-9-ethylthiazalo[3', 2': 2, 3]-as-triazino[5, 6-b]indole 6 and not the isomer, 1-aryl-9-ethylthiazalo[2', 3': 3,4]-as-triazino[5, 6-b]indole 8. The unequivocal synthesis of 8 has also been accomplished. The antibacterial and antifungal activity of the compound 6 has also been evaluated.  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.41B(03) [March 2002]en_US
dc.titleCondensed bridgehead nitrogen heterocyclic systems:Synthesis and antimicrobial activity of thiazolo[3', 2': 2, 3]-as-triazino[5,6-b]indoles and isomeric thiazolo[2', 3': 3,4]-as-triazino[5, 6-b]indolesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.41B(03) [March 2002]

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