Please use this identifier to cite or link to this item: http://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/4885
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dc.contributor.authorBasawaraj, R
dc.contributor.authorNaubade, K
dc.contributor.authorSangapure, SS
dc.date.accessioned2020-06-12T15:05:31Z-
dc.date.available2020-06-12T15:05:31Z-
dc.date.issued2008
dc.identifier.citationINDIAN JOURNAL OF HETEROCYCLIC CHEMISTRY , Vol. 17 , 3 , p. 217 - 220en_US
dc.identifier.urihttp://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/4885-
dc.description.abstractClaisen-Schmidt condensation of 5-chloro-3-methyl-2-acetylbenzofuran 1 with aromatic aldehydes in presence of strong alkali gave 5-chloro-3-methyl-2-arylidene acetylbenzofurans 2-6. Reactions of 2-6 with orthophenylenediamine and orthoaminothiophenol in dry toluene yielded 4-aryl-3-(5'-chloro-3'-methylbenzofuran-2'-yl)-1H benzodiazepines 7-11 and 2-aryl-3- (5'-chloro-3'-methylbenzofuran-2'-yl)-1,5-dihydrothiazepines 12-16. All newly synthesized compounds were evaluated for their antimicrobial, hypnotic and anticonvulsant activities.en_US
dc.publisherDR R S VARMA
dc.titleSynthesis of some benzodiazepines and benzothiazepines bearing benzofuran moiety as possible cns depressants(#)en_US
dc.typeArticle
Appears in Collections:1. Journal Articles

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