Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/9121
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dc.contributor.authorReddy, Y Thirupathi-
dc.contributor.authorReddy, P Narsimha-
dc.contributor.authorKumar, B Sunil-
dc.contributor.authorRao, G V P-
dc.contributor.authorRajitha, B-
dc.date.accessioned2010-05-31T09:56:11Z-
dc.date.available2010-05-31T09:56:11Z-
dc.date.issued2005-06-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/9121-
dc.description1304-1306en_US
dc.description.abstractDihydropyrimidines are prepared by a one-pot cyclo­con­densation of aldehydes, β-ketoesters and urea in acetonitrile by using bismuth oxide perchlorate as the catalyst for the first time is described. Compared to the classical Biginelli reaction conditions, this new method consistently has the advantage of excellent yields (85-95%) and short reaction time (2-4 hr) at lower temperature (40-50oC).en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.relation.ispartofseriesInt.Cl.7 C 07 D 239/00en_US
dc.sourceIJC-B Vol.44B(06) [June 2005]en_US
dc.titleBismuth oxide perchlorate catalysed efficient synthesis of 3,4-dihydropyrimidin-2(1H)-ones: An improved high yielding protocol for the Biginelli reactionen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.44B(06) [June 2005]

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