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Please use this identifier to cite or link to this item: http://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/5557
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dc.contributor.authorHIREMATH, SP
dc.contributor.authorJIVANAGI, AS
dc.contributor.authorPUROHIT, MG
dc.date.accessioned2020-06-12T15:08:14Z-
dc.date.available2020-06-12T15:08:14Z-
dc.date.issued1993
dc.identifier.citationINDIAN JOURNAL OF CHEMISTRY SECTION B-ORGANIC CHEMISTRY INCLUDING MEDICINAL CHEMISTRY , Vol. 32 , 6 , p. 662 - 667en_US
dc.identifier.urihttp://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/5557-
dc.description.abstract3,6-Dimethyl-4-hydrazinocarbonyl-5-(indol-3-yl) pyridazines (2a-d), 3-alkoxycarbonyl-2,5-dime-thyl-4-(indol-3-yl) furans (3a-h). 3-alkoxycarbonyl-2,5-dimethyl-N-substituted (indol-3-yl) pyrroles (4a-h and 5a-h) and 3-acetyl-2,5-dimethyl-4-(indol-3-yl) furans (6a-d) are prepared in one step by the reaction of 2-nitro-1-(indol-3-yl) propenes (1a-d) with ethyl acetoacetate and hydrazine hydrate, methyl/ethyl acetoacetate and triethylamine, methyl/ethyl acetoacetate and n-butylamine/benzylamine, and acetylacetone and piperidine, respectively, in good yields. A few selected compounds are screened for their antibacterial, antifungal, insecticidal, anthelmintic and MAO inhibitor studies.en_US
dc.publisherCOUNCIL SCIENTIFIC INDUSTRIAL RESEARCH
dc.titleSYNTHESIS AND BIOLOGICAL STUDIES OF INDOLYL-PYRIDAZINES, INDOLYL-FURANS AND INDOLYL-PYRROLESen_US
dc.typeArticle
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