Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/60038
Full metadata record
DC FieldValueLanguage
dc.contributor.authorSaikia, Tulan Chandra-
dc.contributor.authorIraqui, Saddam-
dc.contributor.authorRashid, Md. Harunar-
dc.date.accessioned2022-07-05T11:10:34Z-
dc.date.available2022-07-05T11:10:34Z-
dc.date.issued2022-06-
dc.identifier.issn2583-1321 (Online); 0019-5103 (Print)-
dc.identifier.urihttp://nopr.niscpr.res.in/handle/123456789/60038-
dc.description573-581en_US
dc.description.abstractHerein, we report a protocol for the conversion of electron-deficient anilines to formanilides at room temperature using ZnO nanoparticles (NPs). The ZnO NPs of different shapes have been synthesized by conventional co-precipitation techniques and are characterized fully using different microscopic, diffractometric and spectroscopic techniques. The developed protocol is simple, green, inexpensive, and highly efficient. The products can be conveniently separated from the reaction mixture without using the conventional tedious and expensive chromatographic techniques. The protocol is effective for a wide range of substituted anilines, aliphatic amines and heterocycles with moderate to excellent yield. The catalyst is highly stable and is reusable up to the 5th cycle without loss of catalytic activity.en_US
dc.language.isoenen_US
dc.publisherNIScPR-CSIR, Indiaen_US
dc.sourceIJC Vol.61(06) [June 2022]en_US
dc.subjectFormanilidesen_US
dc.subjectheterogeneous catalysten_US
dc.subjectC–N bond formationen_US
dc.subjectnanoparticlesen_US
dc.subjectzinc oxideen_US
dc.titleZnO nanoparticles catalyzed C–N bond-forming reactions: A highly efficient protocol to convert electron-deficient anilines to formanilidesen_US
dc.typeArticleen_US
Appears in Collections:IJC Vol.61(06) [June 2022]

Files in This Item:
File Description SizeFormat 
IJC 61(6) 573-581.pdfMain Article2.3 MBAdobe PDFView/Open
IJC 61(6) 573-581 Suppl. Data.pdfSupplementary Data848.19 kBAdobe PDFView/Open


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