Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/60031
Full metadata record
DC FieldValueLanguage
dc.contributor.authorChalla, Pradeep Kumar-
dc.contributor.authorEga, Jagadeesh Kumar-
dc.date.accessioned2022-07-05T10:43:20Z-
dc.date.available2022-07-05T10:43:20Z-
dc.date.issued2022-06-
dc.identifier.issn2583-1321 (Online); 0019-5103 (Print)-
dc.identifier.urihttp://nopr.niscpr.res.in/handle/123456789/60031-
dc.description635-639en_US
dc.description.abstractThe hydrazones 5 on oxidative cyclization of with [PhI(OAc)2] in the solid state at room temperature under grinding conditions has furnished the respective 2-aryl-5-[2-(3,4,5-trimethoxyphenyl)[1,8]naphthyridin-3-yl]-1,3,4-oxadiazoles 6 in good yields without any undesirable byproducts. The purity of the products is high. The method is preoperatively convenient, useful and environmentally benign. The experimental procedure is very simple and avoids sophistication. The most probable mechanism of above transformation is suggested. The structure of compounds 5 and 6 has been confirmed by their spectroscopic(IR, 1H NMR and MS) and analytical data.en_US
dc.language.isoenen_US
dc.publisherNIScPR-CSIR, Indiaen_US
dc.sourceIJC Vol.61(06) [June 2022]en_US
dc.subject1,8-Naphthyridineen_US
dc.subjectPhI(OAc)2en_US
dc.subjectSiO2-FeCl3en_US
dc.subjectOxadiazolesen_US
dc.titleHypervalent iodine mediated solid state synthesis of 2-aryl-5- [2-(3,4,5-trimethoxyphenyl)[1,8]naphthyridin- 3-yl]-1,3,4-oxadiazolesen_US
dc.typeArticleen_US
Appears in Collections:IJC Vol.61(06) [June 2022]

Files in This Item:
File Description SizeFormat 
IJC 61(6) 635-639.pdf5.06 MBAdobe PDFView/Open


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