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Please use this identifier to cite or link to this item: http://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/5083
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dc.contributor.authorBasawaraj, R
dc.contributor.authorParameshwarappa, G
dc.contributor.authorSangapure, SS
dc.date.accessioned2020-06-12T15:06:10Z-
dc.date.available2020-06-12T15:06:10Z-
dc.date.issued2006
dc.identifier.citationINDIAN JOURNAL OF HETEROCYCLIC CHEMISTRY , Vol. 16 , 1 , p. 75 - 76en_US
dc.identifier.urihttp://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/5083-
dc.description.abstractThe bromination of 5-chloro-3-methyl-2-acetylbenzofuran (1) with bromine in acetic acid gave 5-chloro-3-methyl-2-bromoacetylbenzofuran (2) which on condensation with various substituted aromatic amines afforded 2-N-arylaminoacetyl-5-chloro-3-methylbenzofurans (3-10). These compounds were screened for their antimicrobial analgesic, antiinflammatory and diuretic activities.en_US
dc.publisherDR R S VARMA
dc.titleSynthesis and biological screening of some new 2-N-arylaminoacetyl-5-chloro-3-methylbenzofuransen_US
dc.typeArticle
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