Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/9192
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dc.contributor.authorKe, Shao-Yong-
dc.contributor.authorWei, Tai-Bao-
dc.contributor.authorXue, Si-Jia-
dc.contributor.authorDuan, Li-Ping-
dc.contributor.authorLi, Jing-Zhi-
dc.date.accessioned2010-06-01T04:15:02Z-
dc.date.available2010-06-01T04:15:02Z-
dc.date.issued2005-09-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/9192-
dc.description1957-1960en_US
dc.description.abstractTen new N'-(4, 6-disubstituted-pyrimidin-2-yl)-N-(5-aryl-2-furoyl)thioureas have been synthesized using PEG-400 as solid-liquid phase transfer catalyst under ultrasonic irradiation. Their structures were exactly confirmed by IR, 1H NMR and elemental analysis. The preliminary biological tests show that compound 7b has better inhibitory activities against root and stalk of dicotyledon plant (such as Amaranthus retroflexus L.) in higher concentration.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.relation.ispartofseriesInt.Cl.7 C 07 Den_US
dc.sourceIJC-B Vol.44B(09) [September 2005]en_US
dc.subjectBioactivityen_US
dc.subjectthiourea derivativesen_US
dc.subjectphase transfer catalysten_US
dc.subjectdicotyledon planten_US
dc.subjectAmaranthus retroflexus Len_US
dc.titlePhase transfer catalyzed synthesis under ultrasonic irradiation and bioactivity of N '-(4, 6-disubstituted-pyrimidin-2-yl)- N-(5-aryl-2-furoyl)thiourea derivativesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.44B(09) [September 2005]

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