Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/59337
Full metadata record
DC FieldValueLanguage
dc.contributor.authorTandel, Hemanshu T-
dc.contributor.authorPatel, Saurabh K-
dc.date.accessioned2022-03-23T09:57:32Z-
dc.date.available2022-03-23T09:57:32Z-
dc.date.issued2022-03-
dc.identifier.issn2583-1321 (Online); 0019-5103 (Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/59337-
dc.description328-335en_US
dc.description.abstractSynthesis of 4-(2,4-dimethoxy-6-(5-substitutedphenylisoxazol-3-yl) pyrido[2,3-d] pyrimidin-7-yl)morpholine has been carried out by reaction of (E)-3-(2,4-dimethoxy-7-morpholinopyrido[2,3-d]pyrimidin-6-yl)-1-substituted phenylprop-2-en-1-one with hydroxylamine hydrochloride analogue to get the compounds 8a-f and synthesis of 4-(2,4-dimethoxy-7-morpholinopyrido[2,3-d]pyrimidin-6-yl)-6-phenylpyrimidin-2-ol with urea to get various hydroxypyrimidine of the studied analogue to get the compounds 9a-f. Structures of all the newly synthesized compounds have been characterized by instrumental method. Representative compounds of the synthesized product series have been tested and evaluated as antimicrobial agents.en_US
dc.language.isoenen_US
dc.publisherNIScPR-CSIR, Indiaen_US
dc.sourceIJC Vol.61(03) [March 2022]en_US
dc.subjectIsoxazoleen_US
dc.subjecthydroxypyrimidineen_US
dc.subjectsynthesisen_US
dc.subjectbiological activityen_US
dc.titleDesign, synthesis and biological potential of some isoxazole and hydroxypyrimidine derivatives containing pyrido [2,3-d] pyrimidine nucleus via chalcone seriesen_US
dc.typeArticleen_US
Appears in Collections:IJC Vol.61(03) [March 2022]

Files in This Item:
File Description SizeFormat 
Indian J Chem, 61, 328-335 (Mar,2022).pdfMain Article636.16 kBAdobe PDFView/Open
Indian J Chem, 61, 328-335 (Mar,2022) Suppl. Data.pdfSupplementary Data762 kBAdobe PDFView/Open


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