Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/21726
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dc.contributor.authorXu, Hui-
dc.contributor.authorWang, Yan-Guang-
dc.date.accessioned2013-10-09T05:46:15Z-
dc.date.available2013-10-09T05:46:15Z-
dc.date.issued2003-10-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/21726-
dc.description2604-2607en_US
dc.description.abstractAn efficient synthesis of 4-aryl-5-substituted-6-methyl-3,4-dihydropyrimidin-2(1H)-ones 4a-n by the reaction of aldehydes 1,1,3-dicarbonyl compounds 2 and urea 3using zinc trifluoromethanesulfonate as a catalyst in refluxing acetonitrile is described. Compared to the classical Biginelli reaction conditions, this new method has the advantages of good yields (71-93%)and short reaction time period (4.5-6.5 hr).en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-B Vol.42B(10) [October 2003]en_US
dc.titleZn(OTf)2-catalyzed three-component, one·pot, condensation reaction: An efficient synthesis of 4-aryl-5-substituted-6-methyl-3,4-dihydropyrimidin-2(1H)-onesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.42B(10) [October 2003]

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