Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/43626
Full metadata record
DC FieldValueLanguage
dc.contributor.authorGou, Gao-Zhang-
dc.contributor.authorWu, Na-
dc.contributor.authorZhang, Ju-Cheng-
dc.contributor.authorShi, Ling-
dc.contributor.authorLiu, Gui-Yang-
dc.contributor.authorLiu, Wei-
dc.contributor.authorMang, Chao-Yong-
dc.contributor.authorChi, Shao-Ming-
dc.date.accessioned2018-02-20T06:27:09Z-
dc.date.available2018-02-20T06:27:09Z-
dc.date.issued2018-02-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/43626-
dc.description181-185en_US
dc.description.abstractThe functional 1,8-naphthyridine copper(I) complex, synthesized through a non-catalyst C(sp3)–H methylenation, catalyzes the cross-coupling reaction of aryl halides with imidazoles, by C―N bond formation. The Cu(I) complex catalyzes the reaction with a low catalyst loading (1%, molar fraction) and cheap base even under aerobic conditions.The procedure tolerates aryl halides with various functional groups(such as methyl, methoxy, acetyl, fluoro, nitrile and nitro groups) and gives the corresponding coupling products in moderate to high yields.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-A Vol.57A(02) [February 2018]en_US
dc.subjectCatalystsen_US
dc.subjectCross-coupling reactionsen_US
dc.subjectN-Arylationen_US
dc.subjectCopper(I) complexen_US
dc.subjectImidazolesen_US
dc.titleFunctional 1,8-naphthyridine copper(I) complex as efficient catalyst for n-arylation of imidazoles coupling reactionsen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.57A(02) [February 2018]

Files in This Item:
File Description SizeFormat 
IJCA 57A(2) 181-185.pdfMain Article309.29 kBAdobe PDFView/Open
IJCA 57A(2) 181-185_Suppl Data.pdfSupplementary Data176.89 kBAdobe PDFView/Open


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