Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/16634
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dc.contributor.authorGadaginamath, G S-
dc.contributor.authorKavali, R R-
dc.contributor.authorPujar, S R-
dc.date.accessioned2013-03-29T19:46:59Z-
dc.date.available2013-03-29T19:46:59Z-
dc.date.issued1999-10-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/16634-
dc.description1226-1228en_US
dc.description.abstract5-Hydroxyindole 1a is reacted with bromine in acetic acid to yield 6-bromo-5-hydroxyindole 1b. Compounds 1a-b are condensed with chloroacetonitrile in refluxing acetone in the presence of K2CO3 to obtain 3-acetyl-1-n-butyl-2-methylindol-5-yloxyacetonitriles 2a-b which are then reacted with dicyanodiamide in the presence of KOH in methanol and isopropanol to obtain the required 1-n-butyl-3-acetyl-5-(2,4-diamino-1,3,5-triazin-6-yl)methoxy-2-methylindoles 3a-b. All these new compounds have been screened for their antibacterial and antifungal activities.  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.38B(10) [October 1999]en_US
dc.titleSynthesis and antimicrobial activity of new 1-n-butyl-3-acetyl-5-(2,4-diamino-1,3,5-triazin-6-yl)methoxy-2-methylindole derivativesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.38B(10) [October 1999]

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