Please use this identifier to cite or link to this item: http://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/5147
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dc.contributor.authorBasawaraj, R
dc.contributor.authorMaddur, S
dc.contributor.authorSangapure, SS
dc.date.accessioned2020-06-12T15:06:18Z-
dc.date.available2020-06-12T15:06:18Z-
dc.date.issued2005
dc.identifier.citationINDIAN JOURNAL OF HETEROCYCLIC CHEMISTRY , Vol. 15 , 2 , p. 153 - 156en_US
dc.identifier.urihttp://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/5147-
dc.description.abstractThe reaction of 5-chloro-3-methyl-2-bromoacetylbenzofuran 2 with various substituted arylthioureas and arylidene thiosemicarbazides in ethanol gave 2-arylamino/arylidene hydrazino-4-(5'-chloro-3'-methylbenzofuran-2'-yl) thiazoles (3a-h) and (4a-e). The compounds have been screened for their antimicrobial, antiinflammatory and diuretic activity.en_US
dc.publisherDR R S VARMA
dc.titleSynthesis and pharmacological activities of some 2-arylamino/arylidene hydrazino-4-(5 '-chloro-3 '-methylbenzofuran-2-yl) thiazolesen_US
dc.typeArticle
Appears in Collections:1. Journal Articles

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