A novel 4-aminoantipyrine-Pd(II) complex catalyzes Suzuki–Miyaura cross-coupling reactions of aryl halides

Scholarly Works

• Fallah-Mehrjardi, M.; Kargar, H.; Munawar, K. S. Tridentate ONO hydrazone Schiff base complexes in organic transformations: Catalytic and mechanistic studies. Inorganica Chimica Acta 2024, 560, 121835. doi:10.1016/j.ica.2023.121835
• Madhura, M. J.; Jeevan Chakravarthy, A. S.; Hariprasad, S.; Gayathri, V. Suzuki–Miyaura Cross Coupling Reaction Using Reusable Polymer Anchored Palladium Catalyst. Catalysis Letters 2022, 153, 1141–1149. doi:10.1007/s10562-022-04055-7
• Rajmane, A.; Jadhav, S. N.; Kumbhar, A. N, O-polydentate ligands for palladium-catalyzed cross-coupling reactions (Part III). Journal of Organometallic Chemistry 2022, 957, 122147. doi:10.1016/j.jorganchem.2021.122147
• Alam, M. S.; Lee, D.-U. Molecular structure, spectral (FT-IR, FT-Raman, Uv-Vis, and fluorescent) properties and quantum chemical analyses of azomethine derivative of 4-aminoantipyrine. Journal of Molecular Structure 2021, 1227, 129512. doi:10.1016/j.molstruc.2020.129512
• Rao, M. L. N.; Meka, S. Pd-catalyzed atom-efficient cross-coupling of triarylbismuth reagents with protecting group-free iodophenylmethanols: Synthesis of biarylmethanols. Tetrahedron Letters 2020, 61, 151676. doi:10.1016/j.tetlet.2020.151676
• Heintges, G. H. L.; Janssen, R. A. J. On the homocoupling of trialkylstannyl monomers in the synthesis of diketopyrrolopyrrole polymers and its effect on the performance of polymer-fullerene photovoltaic cells. RSC advances 2019, 9, 15703–15714. doi:10.1039/c9ra02670c
• Fathima, S. S. A.; Paulpandiyan, R.; Nagarajan, E. R. Expatiating biological excellence of aminoantipyrine derived novel metal complexes: Combined DNA interaction, antimicrobial, free radical scavenging studies and molecular docking simulations. Journal of Molecular Structure 2019, 1178, 179–191. doi:10.1016/j.molstruc.2018.10.021
• Barbero, M.; Dughera, S. Gold catalysed Suzuki-Miyaura coupling of arenediazonium o-benzenedisulfonimides. Tetrahedron 2018, 74, 5758–5769. doi:10.1016/j.tet.2018.08.018
• Camacho, A. S.; Martín-García, I.; Contreras-Celedón, C.; Chacón-García, L.; Alonso, F. DNA-supported palladium nanoparticles as a reusable catalyst for the copper- and ligand-free Sonogashira reaction. Catalysis Science & Technology 2017, 7, 2262–2273. doi:10.1039/c7cy00001d
• Schmidt, B.; Riemer, M. Microwave-Promoted Pd-Catalyzed Synthesis of Dibenzofurans from Ortho-Arylphenols. Journal of Heterocyclic Chemistry 2016, 54, 1287–1297. doi:10.1002/jhet.2704
• Nikoorazm, M.; Ghorbani-Choghamarani, A.; Khanmoradi, M. Immobilization of palladium on functionalized nanoporous MCM-41 and its application in C–C bond-forming and synthesis of DHQs. Journal of Porous Materials 2016, 23, 761–772. doi:10.1007/s10934-016-0131-1
• Ghorbani-Choghamarani, A.; Norouzi, M. Palladium supported on modified magnetic nanoparticles: a phosphine‐free and heterogeneous catalyst for Suzuki and Stille reactions. Applied Organometallic Chemistry 2015, 30, 140–147. doi:10.1002/aoc.3409
• Alam, M. S.; Lee, D.-U. Novel Fluorescent Schiff Base Derivatives of 4‐Aminoantipyrine with Large Stokes Shifts and Dual Emission Properties: Crystal Structure, Molecular Interactions, Molecular Surfaces, Conformational and DFT Analyses. Bulletin of the Korean Chemical Society 2015, 36, 2415–2428. doi:10.1002/bkcs.10464
• Premnath, D.; Selvakumar, P. M.; Ravichandiran, P.; Selvan, G. T.; Indiraleka, M.; Vennila, J. J. Synthesis and spectroscopic characterization of fluorescent 4-aminoantipyrine analogues: Molecular docking and in vitro cytotoxicity studies. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 2015, 153, 118–123. doi:10.1016/j.saa.2015.08.008
• Contreras-Celedón, C.; Rincon‐Medina, J. A.; Mendoza-Rayo, D.; Chacón-García, L. Oxidative homocoupling of arylboronic acids catalyzed by a 4‐aminoantipyrine–Pd(II)complex. Applied Organometallic Chemistry 2015, 29, 439–442. doi:10.1002/aoc.3312

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