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DC Field | Value | Language |
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dc.contributor.author | Hiremath, SP | |
dc.contributor.author | Rudresh, K | |
dc.contributor.author | Saundane, AR | |
dc.date.accessioned | 2020-06-12T15:08:46Z | - |
dc.date.available | 2020-06-12T15:08:46Z | - |
dc.date.issued | 2002 | |
dc.identifier.citation | INDIAN JOURNAL OF CHEMISTRY SECTION B-ORGANIC CHEMISTRY INCLUDING MEDICINAL CHEMISTRY , Vol. 41 , 2 , p. 394 - 399 | en_US |
dc.identifier.uri | http://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/5776 | - |
dc.description.abstract | 10-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.publisher | NATL INST SCIENCE COMMUNICATION | |
dc.title | Synthesis 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 pyrazolines | en_US |
dc.type | Article | |
Appears in Collections: | 1. Journal Articles |
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