Devi, Elangbam PinkyKant, KamalKaldhi, DhananjayaGhanta, SusantaSengupta, RaginiAl-Zaqri, NabilSingh, VirenderMalakar, Chandi C.2024-01-212024-08-132024-01-212024-08-132023-09-141040663810.1080/10406638.2023.2257841http://10.2.3.109/handle/32116/3290An 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-USamidesC-N bond formationDFT analysisNH<sub>2</sub>OH?HCl reagentTransamidationMetal- and Hazardous Reagent-Free Transamidation Process: the NH2OH?HCl Promoted N-Formylation and N-Acylation Reaction under Solvent-Less ConditionsArticlehttps://www.tandfonline.com/doi/full/10.1080/10406638.2023.2257841Polycyclic Aromatic Compounds