The γ-Valerolactone (GVL) as Innoxious Reaction Media for the Synthesis of 2-Aryl-2H-Indazoles via C-N and N-N Bond Formation under Cu(I)-Catalyzed Ligand and Base Free Conditions

dc.contributor.authorSingh, L.S.
dc.contributor.authorKant, K.
dc.contributor.authorBanerjee, S.
dc.contributor.authorSengupta, R.
dc.contributor.authorAlObaid, A.A.
dc.contributor.authorPal, M.
dc.contributor.authorDutta, S.
dc.contributor.authorAljaar, N.
dc.contributor.authorMalakar, C.C.
dc.date.accessioned2026-02-04T12:25:42Z
dc.date.issued2024
dc.description.abstractAn efficient method for N-arylation and N-N bond formation has been developed using an innoxious reaction medium, γ-valerolactone (GVL), as both a solvent and a ligand. The strategy involves utilizing CuI as a catalyst under conditions free of external ligands and bases. Various aldehyde and amine derivatives with different functional groups were investigated, resulting in the production of 2-aryl-2H-indazole compounds with yields ranging from 75% to 93%. This study highlights the effectiveness of GVL, a solvent derived from biomass, as a reaction medium and ligand in a multicomponent reaction. © 2023 Taylor & Francis Group, LLC.
dc.identifier.citationPolycyclic Aromatic Compounds, 2024, 44, 7, pp. 4832-4843
dc.identifier.issn10406638
dc.identifier.urihttps://doi.org/10.1080/10406638.2023.2257846
dc.identifier.urihttps://idr.nitk.ac.in/handle/123456789/21493
dc.publisherTaylor and Francis Ltd.
dc.subjectChelation
dc.subjectCopper compounds
dc.subjectLigands
dc.subjectReaction kinetics
dc.subject2h-indazole
dc.subjectBond formation
dc.subjectC-N bond formation
dc.subjectCu(I)-catalyse
dc.subjectIndazole
dc.subjectMulticomponent reaction
dc.subjectMulticomponents
dc.subjectN-N bond formation
dc.subjectReaction media
dc.subjectCatalysis
dc.titleThe γ-Valerolactone (GVL) as Innoxious Reaction Media for the Synthesis of 2-Aryl-2H-Indazoles via C-N and N-N Bond Formation under Cu(I)-Catalyzed Ligand and Base Free Conditions

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