Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/7072
Full metadata record
DC FieldValueLanguage
dc.contributor.authorKataki, Dolly-
dc.contributor.authorChakraborty, Pranita-
dc.contributor.authorSarmah, Pubalee-
dc.contributor.authorPhukan, Prodeep-
dc.date.accessioned2010-01-05T10:30:54Z-
dc.date.available2010-01-05T10:30:54Z-
dc.date.issued2006-09-
dc.identifier.issn0975-0991 (Online); 0971-457X (Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/7072-
dc.description519-521en_US
dc.description.abstractAn improved solvent free, one pot procedure for the synthesis of 5-ethoxycarbonyl-4-aryl-3,4-dihydropyrimidin-2(1H)-ones catalyzed by iodine is developed. The process has been utilized successfully in large-scale synthesis of Biginelli products.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.relation.ispartofseriesC07D239/00en_US
dc.sourceIJCT Vol.13(5) [September 2006]en_US
dc.subjectIodineen_US
dc.subjectAldehydeen_US
dc.subjectEthyl acetoacetateen_US
dc.subjectUreaen_US
dc.subjectDihydropyrimidin-2(1H)-oneen_US
dc.subjectSolvent free conditionen_US
dc.titleScalable synthesis of 3,4-dihydropyrimidin-2(1H)-ones under solvent free conditionen_US
dc.typeArticleen_US
Appears in Collections:IJCT Vol.13(5) [September 2006]

Files in This Item:
File Description SizeFormat 
IJCT 13(5) 519-521.pdf39.46 kBAdobe PDFView/Open


Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.