Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/3414
Full metadata record
DC FieldValueLanguage
dc.contributor.authorThunga, Sanjeeva-
dc.contributor.authorSingh, Neetika-
dc.contributor.authorAnugu, Naveenkumar-
dc.contributor.authorKokatla, Hari Prasad-
dc.date.accessioned2025-10-23T05:59:13Z-
dc.date.available2025-10-23T05:59:13Z-
dc.date.issued2024-
dc.identifier.citation10.1021/acs.joc.4c02050en_US
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/3414-
dc.descriptionNITWen_US
dc.description.abstractRongalite-mediated one-pot aminomethylation of heteroarenes using secondary amines/anilines has been developed. This transition-metal-free and mild reaction offers an efficient way to synthesize aminomethylated heteroaromatic compounds with high yields and broad functional group tolerance. Here, Rongalite plays a key role in generating the C1 unit source in situ, which triggers the aminomethylation process. This approach provides a library of aminomethylated imidazo[1,2-a]pyridines and imidazo[2,1-b]- thiazoles.en_US
dc.language.isoenen_US
dc.publisherThe Journal of Organic Chemistryen_US
dc.subjectRongaliteen_US
dc.titleOne-Pot Aminomethylation of Heteroarenes by Rongalite as In Situ C1 Sourceen_US
dc.typeArticleen_US
Appears in Collections:Chemistry

Files in This Item:
File Description SizeFormat 
23. J.Org.Chem.2024,89,18649−18653.pdf1.63 MBAdobe PDFView/Open


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