Please use this identifier to cite or link to this item: http://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/5776
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dc.contributor.authorHiremath, SP
dc.contributor.authorRudresh, K
dc.contributor.authorSaundane, AR
dc.date.accessioned2020-06-12T15:08:46Z-
dc.date.available2020-06-12T15:08:46Z-
dc.date.issued2002
dc.identifier.citationINDIAN JOURNAL OF CHEMISTRY SECTION B-ORGANIC CHEMISTRY INCLUDING MEDICINAL CHEMISTRY , Vol. 41 , 2 , p. 394 - 399en_US
dc.identifier.urihttp://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/5776-
dc.description.abstract10-Substituted-6H, 7H-indolo[2, 3-c]isoquinolin-5-thiones 2a-c are reacted with hydrazine hydrate to yield the corresponding 5-hydrazino-10-substituted-7H-indolo[2, 3-c]isoquinolines 3a-c. These hydrazines on cyclodehydration with acetyl acetone, ethyl acetoacetate and arylidene acetophenones in acidic medium furnish the respective pyrazoles 4a-c, pyrazolones 5a-c and 3, 5-disubstituted pyrazolines 6a-c. These previously unknown compounds have been screened for their antimicrobial, analgesic and antiinflammatory activities.en_US
dc.publisherNATL INST SCIENCE COMMUNICATION
dc.titleSynthesis and biological activities of new 5-hydrazino-10-substituted-7H-indolo[2, 3-c]isoquinolines and 1-(10-substituted-7H-indolo[2, 3-c]isoquinolin-5yl)-3,5-disubstituted pyrazoles,-3-methyl pyrazol-5-ones and-3, 5-disubstituted pyrazolinesen_US
dc.typeArticle
Appears in Collections:1. Journal Articles

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