Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/18806
Full metadata record
DC FieldValueLanguage
dc.contributor.authorRajanarendar, E-
dc.contributor.authorRamu, K-
dc.contributor.authorSrinivas, M-
dc.date.accessioned2013-06-07T09:46:11Z-
dc.date.available2013-06-07T09:46:11Z-
dc.date.issued2004-08-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/18806-
dc.description1784-1786en_US
dc.description.abstractTrimolecular condensation of N-(5-methyl-3- isoxazolyl)- N'-aryl ureas 2 with aqueous formaldehyde and primary amines under microwave irradiation in ethanol leads to 5-alkyl-1-(5-methylisoxazol-3-yl)-3-aryl-[1,3,5] triazinan-2-ones 3 in excellent yields. The intermediates, N-(5-methyl-3- isoxazolyl)-N'-aryl thioureas 2, have been obtained by reaction of 3-amino-5-methylisoxazole 1 with arylisocyanates in toluene under microwave irradiation.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.relation.ispartofseriesInt.Cl.7 C 07 D 261/00, 251/00en_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-B Vol.43B(08) [August 2004]en_US
dc.titleMicrowave assisted synthesis of some new isoxazolyltriazinan-2-oneszen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.43B(08) [August 2004]

Files in This Item:
File Description SizeFormat 
IJCB 43B(8) 1784-1786.pdf658.98 kBAdobe PDFView/Open


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