Please use this identifier to cite or link to this item: https://idr.nitk.ac.in/jspui/handle/123456789/13198
Full metadata record
DC FieldValueLanguage
dc.contributor.authorMange, Y.J.
dc.contributor.authorIsloor, A.M.
dc.contributor.authorMalladi, S.
dc.contributor.authorIsloor, S.
dc.contributor.authorFun, H.-K.
dc.date.accessioned2020-03-31T08:45:22Z-
dc.date.available2020-03-31T08:45:22Z-
dc.date.issued2013
dc.identifier.citationArabian Journal of Chemistry, 2013, Vol.6, 2, pp.177-181en_US
dc.identifier.urihttp://idr.nitk.ac.in/jspui/handle/123456789/13198-
dc.description.abstractIn the present investigation, a series of new Schiff bases 4a-f were synthesized by the condensation of N-[(4-amino-5-sulfanyl-4. H-1,2,4-triazol-3-yl)methyl]-4-substituted-benzamides 3a-b with various substituted aromatic aldehydes in ethanol-dioxane mixture using catalytic amount of sulfuric acid. The starting materials 3a-b were in turn synthesized by the fusion of benzoyl glycine/substituted benzoylglycine with thiocarbohydrazide. Newly synthesized compounds were characterized by IR, NMR, mass spectra and elemental analyses. All the compounds were evaluated for their antibacterial and antifungal activity using the Minimum Inhibition Concentration (MIC) method by serial dilution technique. Few of the compounds were found to be biologically active. 2011.en_US
dc.titleSynthesis and antimicrobial activities of some novel 1,2,4-triazole derivativesen_US
dc.typeArticleen_US
Appears in Collections:1. Journal Articles

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.