Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/21827
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dc.contributor.authorMohan, Jag-
dc.date.accessioned2013-10-10T11:03:12Z-
dc.date.available2013-10-10T11:03:12Z-
dc.date.issued2002-02-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/21827-
dc.description403-406en_US
dc.description.abstractThe synthesis of 2-p-fluorophcnyl-5-p-bromophenylthiazolo[3,2-b]-s-triazole 5 has been achieved starting from 3-p-fluorophenyl-5-mercapto-s-triazole 3. Compound 3 on condensation with p-bromophenacyl bromide gave the ketone 4 which on cyclization with PPA affords thiazolo[3,2-b]-s-triazole 5 and not the isomeric thiazolo[2,3-c]-s-triazole 7. This has been established by an unequivocal synthesis of 7 through POCl3 cyclization of 2-p-fluorobenzoylhydrazino-4-pbromophenyl thiazole hydrobromide 6. However the condensation of 4-amino-5-mercapto-3-p-fluorophenyl-s-triazole 8 with p-chlorophenacyl bromide furnishes 7H-6-p-chlorophenyl-3-p-fluorophenyl-s-triazolo[3,4,-b] [1,3,4] thi adiazine 9 in one step only. The diuretic, antibacterial and antifungal activities of these compounds have 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(02) [February 2002]en_US
dc.titleCondensed heterocyclic systems containing bridgehead nitrogen atom: Synthesis and antimicrobial activity of s-triazolo[3,4-b][1, 3,4] thiadiazines, thiazolo[3,2-b]-s-triazoles and isomeric thiazolo[2,3-c]-s-triazolesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.41B(02) [February 2002]

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