Metal- and Hazardous Reagent-Free Transamidation Process: the NH2OH?HCl Promoted N-Formylation and N-Acylation Reaction under Solvent-Less Conditions

dc.contributor.authorDevi, Elangbam Pinky
dc.contributor.authorKant, Kamal
dc.contributor.authorKaldhi, Dhananjaya
dc.contributor.authorGhanta, Susanta
dc.contributor.authorSengupta, Ragini
dc.contributor.authorAl-Zaqri, Nabil
dc.contributor.authorSingh, Virender
dc.contributor.authorMalakar, Chandi C.
dc.date.accessioned2024-01-21T10:33:11Z
dc.date.accessioned2024-08-13T11:16:22Z
dc.date.available2024-01-21T10:33:11Z
dc.date.available2024-08-13T11:16:22Z
dc.date.issued2023-09-14T00:00:00
dc.description.abstractAn efficient transamidation process has been described under solvent-less conditions. The transformation has been accomplished by employing NH2OH?HCl as a reagent and amines as substrates. The developed method is achieved in the absence of metals and hazardous reagents. A series of amines were explored to obtain the N-formylation and N-acylation reactions with excellent yields (81-96%) of products. The DFT analysis was also performed, which provides a clear understanding of the described N-formylation process. The postulated mechanism is well supported by the control experiments. � 2023 Taylor & Francis Group, LLC.en_US
dc.identifier.doi10.1080/10406638.2023.2257841
dc.identifier.issn10406638
dc.identifier.urihttps://kr.cup.edu.in/handle/32116/3290
dc.identifier.urlhttps://www.tandfonline.com/doi/full/10.1080/10406638.2023.2257841
dc.language.isoen_USen_US
dc.publisherTaylor and Francis Ltd.en_US
dc.subjectamidesen_US
dc.subjectC-N bond formationen_US
dc.subjectDFT analysisen_US
dc.subjectNH<sub>2</sub>OH?HCl reagenten_US
dc.subjectTransamidationen_US
dc.titleMetal- and Hazardous Reagent-Free Transamidation Process: the NH2OH?HCl Promoted N-Formylation and N-Acylation Reaction under Solvent-Less Conditionsen_US
dc.title.journalPolycyclic Aromatic Compoundsen_US
dc.typeArticleen_US
dc.type.accesstypeClosed Accessen_US

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