Please use this identifier to cite or link to this item: http://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/5015
Full metadata record
DC FieldValueLanguage
dc.contributor.authorParameshwarappa G
dc.contributor.authorLingamani J
dc.contributor.authorPatil S.B
dc.contributor.authorGoudgaon N.M.
dc.date.accessioned2020-06-12T15:05:57Z-
dc.date.available2020-06-12T15:05:57Z-
dc.date.issued2009
dc.identifier.citationHeterocyclic Communications , Vol. 15 , 5 , p. 343 - 348en_US
dc.identifier.urihttp://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/5015-
dc.description.abstractA series of some innovative 7-((4-substituted thiazol-2-yl) metiioxy)-4-memyl-2H-chromen-2-one (4a-d) & (6a-b) were syntiiesized starting from ethyl 2-(4-methyl-2-oxo-2H-chromone-7-yloxy)acetate (la). Reaction of compound (la) with aqueous ammonia yielded 2-(4-methyl-2-oxo-2H-chromomen-7- yloxy)acetamide (2a). Compound (2a) on reaction with P2S5 in dioxane gave 2-(4-methyl-2-oxo-2H-chromomen-7yloxy) ethanethioamide (3a). Reaction of (3a) with different substituted phenacylbromide/ dichloroacetone afforded (4a-d) & (5a). Condensation of (5a) with different secondary amines gave desired compounds (6a-b). The newly synthesized compounds are characterized by IR, 1H NMR and mass spectral studies. These synthesized compounds were also screened for their antibacterial and antifungal activities.en_US
dc.subject2,4-disubtituted thiazoles
dc.subject2-(4-methyl-2-oxo-2h-chromomen-7yloxy)ethanemioamide
dc.subjectAnti-microbial activity
dc.titleSynthesis and anti-microbial activity of thiazole substituted coumarinsen_US
dc.typeArticle
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.