Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/6231
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dc.contributor.authorMing, Li-
dc.contributor.authorLirong, Wen-
dc.contributor.authorXiao, Wang-
dc.contributor.authorChangsheng, Yao-
dc.contributor.authorWeijun, Fu-
dc.contributor.authorGuilong, Zhao-
dc.contributor.authorFangzhong, Hu-
dc.contributor.authorHuazheng, Yang-
dc.date.accessioned2009-10-21T04:43:28Z-
dc.date.available2009-10-21T04:43:28Z-
dc.date.issued2006-02-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/6231-
dc.description483-488en_US
dc.description.abstractTen biologically active trifluoromethyl containing N-substituted-benzoylpyrazoles (3a-d, 4a-d, and 6a, b) and one triazole analogue 5 have been conveniently synthesized from four versatile polyfunctionalized ethylene synthons and one novel synthon N-cyanoimido-S,S- dimethyldithio-carbonate (CIDT, v), respectively. The reactions of trifluoromethyl containing substituted benzoylhydrazine with classical synthons such as ethyl dimethylaminomethylene- malonate, acetylacetone and ethyl acetoacetate have also been investigated. Herbicidal, fungicidal and plant-growth regulation activities for all reported new compounds have been determined and reported.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.relation.ispartofseriesInt.Cl.7 C 07 Den_US
dc.sourceIJC-B Vol.45B(02) [February 2006]en_US
dc.subjectbiological activityen_US
dc.subjectpyrazoleen_US
dc.subjecttriazoleen_US
dc.subjectsynthonen_US
dc.subjectsynthesisen_US
dc.titleUse of polyfunctionalized ethylene synthons: Convenient synthesis of biologically active trifluoromethyl containing N-substituted-benzoylpyrazoles and triazoleen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.45B(02) [February 2006]

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