Works matching DE "QUINOLINE derivatives"
Results: 629
A novel thermoregulated phase-separable Pt nanocatalyst for selective hydrogenation of quinoline and its derivatives.
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- Journal of Chemical Research, 2025, v. 49, n. 1, p. 1, doi. 10.1177/17475198241311697
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Antitubercular activity of silver(I) complexes with 7-chloro-4-aminoquinolines: synthesis, characterization and in vitro biological assays.
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- Journal of Coordination Chemistry, 2025, v. 78, n. 4, p. 409, doi. 10.1080/00958972.2024.2448518
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Synchronous Proton‐Hydride Transfer by a Pyrazole‐Functionalized Protic Mn(I) Complex in Catalytic Alcohol Dehydrogenative Coupling.
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- Chemistry - A European Journal, 2023, v. 29, n. 58, p. 1, doi. 10.1002/chem.202301758
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Phosphine‐Functionalized Syndiotactic Polystyrenes: Synthesis and Application to Immobilization of Transition Metal Nanoparticle Catalysts.
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- Chemistry - A European Journal, 2022, v. 28, n. 62, p. 1, doi. 10.1002/chem.202202113
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Circularly Polarized Room Temperature Phosphorescence through Twisting‐Induced Helical Structures from Polyvinyl Alcohol‐Based Fibers Containing Hydrogen‐Bonded Dyes.
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- Angewandte Chemie, 2024, v. 136, n. 29, p. 1, doi. 10.1002/ange.202403391
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- Article
Jiajia Ma.
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- Angewandte Chemie, 2024, v. 136, n. 4, p. 1, doi. 10.1002/ange.202317837
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- Article
Adaptive Catalysts for the Selective Hydrogenation of Bicyclic Heteroaromatics using Ruthenium Nanoparticles on a CO<sub>2</sub>‐Responsive Support.
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- Angewandte Chemie, 2023, v. 135, n. 48, p. 1, doi. 10.1002/ange.202311427
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Site‐Selective Electrochemical C−H Carboxylation of Arenes with CO<sub>2</sub>.
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- Angewandte Chemie, 2023, v. 135, n. 3, p. 1, doi. 10.1002/ange.202214710
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Visible Light‐Mediated Cyclisation Reaction for the Synthesis of Highly‐Substituted Tetrahydroquinolines and Quinolines.
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- Angewandte Chemie, 2023, v. 135, n. 2, p. 1, doi. 10.1002/ange.202207829
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Transition‐Metal‐Free Synthesis of Functionalized Quinolines by Direct Conversion of β‐O‐4 Model Compounds.
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- Angewandte Chemie, 2022, v. 134, n. 38, p. 1, doi. 10.1002/ange.202206284
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Catalytic Asymmetric Halogenation/Semipinacol Rearrangement of 3‐Hydroxyl‐3‐vinyl Oxindoles: A Stereodivergent Kinetic Resolution Process.
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- Angewandte Chemie, 2021, v. 133, n. 51, p. 26803, doi. 10.1002/ange.202110315
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- Article
Hydrogen‐Bonding‐Promoted Cascade Rearrangement Involving the Enlargement of Two Rings: Efficient Access to Polycyclic Quinoline Derivatives.
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- Angewandte Chemie, 2020, v. 132, n. 48, p. 21609, doi. 10.1002/ange.202008110
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Dearomative Photocatalytic Construction of Bridged 1,3‐Diazepanes.
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- Angewandte Chemie, 2020, v. 132, n. 10, p. 4150, doi. 10.1002/ange.201914390
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Acyl Migration versus Epoxidation in Gold Catalysis: Facile, Switchable, and Atom‐Economic Synthesis of Acylindoles and Quinoline Derivatives.
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- Angewandte Chemie, 2020, v. 132, n. 1, p. 479, doi. 10.1002/ange.201912334
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The effects of co-sensitization in dye-sensitized solar cells.
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- Journal of Materials Science, 2013, v. 48, n. 9, p. 3448, doi. 10.1007/s10853-013-7134-y
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Synthesis, Hydrolysis, and Analgesic Activity of 3-[3-(1-arylethylcarbamoyl)-4-hydroxy-2-oxo-1,2-dihydroquinolin-1-yl]propanenitriles and Their Derivatives.
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- Pharmaceutical Chemistry Journal, 2016, v. 50, n. 7, p. 431, doi. 10.1007/s11094-016-1464-4
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Synthesis and Neurotropic Activity of Amino Derivatives of Cyclopenta[4′,5′]pyrido[3′,2′:4,5]thieno[3,2- d ]pyrimidines and Pyrimido[4′,5′:4,5]thieno[2,3- c]isoquinolines.
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- Pharmaceutical Chemistry Journal, 2016, v. 50, n. 5, p. 301, doi. 10.1007/s11094-016-1440-z
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- Article
Synthesis and Neurotropic Activity of New Pyrimido[4′,5′:4,5]Thieno[2,3- b]Quinoline Derivatives.
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- Pharmaceutical Chemistry Journal, 2015, v. 49, n. 9, p. 587, doi. 10.1007/s11094-015-1334-5
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Synthesis and Antioxidant Activity of Tricyclic Compounds Containing a 5,6,7,8-Tetrahydroquinoline Moiety.
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- Pharmaceutical Chemistry Journal, 2014, v. 48, n. 2, p. 100, doi. 10.1007/s11094-014-1057-z
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Relationship between the structure and physicochemical characteristics of 1,2,3,4-tetrahydroquinoline derivatives.
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- Journal of Structural Chemistry, 2017, v. 58, n. 4, p. 767, doi. 10.1134/S0022476617040187
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- Article
The structure of a novel 8-hydroxyquinoline ligand system including 1,3-tropolonic fragment.
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- Journal of Structural Chemistry, 2016, v. 57, n. 8, p. 1688, doi. 10.1134/S0022476616080291
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- Article
Synthesis and Antioxidant Properties of Novel Fluorescein-Based Quinoline Glycoconjugates.
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- Journal of Carbohydrate Chemistry, 2014, v. 33, n. 3, p. 137, doi. 10.1080/07328303.2014.897351
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Advances in polymer based Friedlander quinoline synthesis.
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- Turkish Journal of Chemistry, 2021, v. 45, n. 5, p. 1299, doi. 10.3906/kim-2106-5
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Synthesis and molecular docking studies of quinoline derivatives as HIV non-nucleoside reverse transcriptase inhibitors.
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- Turkish Journal of Chemistry, 2020, v. 44, n. 6, p. 1623, doi. 10.3906/kim-2004-14
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Innovational combination of hetero-bifunctional N-PEG quinoline scaffolds derivatives with improved anticancer activity against breast and colon cancer cell lines and P-glycoprotein, cytochrome p450 enzyme activity prediction.
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- Turkish Journal of Chemistry, 2020, v. 44, n. 6, p. 1495, doi. 10.3906/kim-2006-13
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Synthesis of 2-substituted 8-propargyloxyquinoline derivatives and determination of their antioxidant, antibacterial, and DNA binding activities.
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- Turkish Journal of Chemistry, 2018, v. 42, n. 5, p. 1358, doi. 10.3906/kim-1805-77
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Synthesis and biological evaluation of quinoline-triazole and quinolone-triazole conjugates.
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- Turkish Journal of Chemistry, 2018, v. 42, n. 5, p. 1344, doi. 10.3906/kim-1804-18
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Simple and convenient preparation of novel 6,8-disubstituted quinoline derivatives and their promising anticancer activities.
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- Turkish Journal of Chemistry, 2013, v. 37, n. 6, p. 896, doi. 10.3906/kim-1301-30
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One Pot Synthesis of "3-(4,5-Diphenyl-1H-Imidazol-2-yl)-2-Phenoxyquinolines" and Their Potential as α-Glucosidase Inhibitors: Molecular Docking and MDS Investigation.
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- Polycyclic Aromatic Compounds, 2024, v. 44, n. 6, p. 4239, doi. 10.1080/10406638.2023.2247122
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New quinoline and isatin derivatives as apoptotic VEGFR-2 inhibitors: design, synthesis, anti-proliferative activity, docking, ADMET, toxicity, and MD simulation studies.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2022, v. 37, n. 1, p. 2191, doi. 10.1080/14756366.2022.2110869
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Discovery of novel quinoline-based analogues of combretastatin A-4 as tubulin polymerisation inhibitors with apoptosis inducing activity and potent anticancer effect.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2021, v. 36, n. 1, p. 802, doi. 10.1080/14756366.2021.1899168
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Discovery of new quinolines as potent colchicine binding site inhibitors: design, synthesis, docking studies, and anti-proliferative evaluation.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2021, v. 36, n. 1, p. 640, doi. 10.1080/14756366.2021.1883598
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Identification of histone deacetylase inhibitors with (arylidene)aminoxy scaffold active in uveal melanoma cell lines.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2021, v. 36, n. 1, p. 34, doi. 10.1080/14756366.2020.1835883
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Design, synthesis, and anticancer evaluation of novel quinoline derivatives of ursolic acid with hydrazide, oxadiazole, and thiadiazole moieties as potent MEK inhibitors.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2019, v. 34, n. 1, p. 955, doi. 10.1080/14756366.2019.1605364
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- Article
Antibacterial activity of 3-methylbenzo[d]thiazol-methylquinolinium derivatives and study of their action mechanism.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2018, v. 33, n. 1, p. 879, doi. 10.1080/14756366.2018.1465055
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Correction to: New cyclopentaquinoline hybrids with multifunctional capacities for the treatment of Alzheimer’s disease.
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- 2018
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- Correction Notice
Synthesis and biological evaluation of N-arylpiperazine derivatives of 4,4-dimethylisoquinoline-1,3(2H,4H)-dione as potential antiplatelet agents.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2018, v. 33, n. 1, p. 536, doi. 10.1080/14756366.2018.1437155
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Synthesis and biological evaluation of 2-styrylquinolines as antitumour agents and EGFR kinase inhibitors: molecular docking study.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2018, v. 33, n. 1, p. 199, doi. 10.1080/14756366.2017.1407926
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New cyclopentaquinoline hybrids with multifunctional capacities for the treatment of Alzheimer’s disease.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2018, v. 33, n. 1, p. 158, doi. 10.1080/14756366.2017.1406485
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Synthesis and preliminary structure-activity relationship study of 2-aryl-2H-pyrazolo[4,3-c]quinolin-3-ones as potential checkpoint kinase 1 (Chk1) inhibitors.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2018, v. 33, n. 1, p. 171, doi. 10.1080/14756366.2017.1404592
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Antitumor activity of amidino-substituted benzimidazole and benzimidazo[1,2- a ]quinoline derivatives tested in 2D and 3D cell culture systems.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1139, doi. 10.3109/14756366.2015.1101093
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Synthesis and in vitro evaluation of 4-substituted furano[3,2-c] tetrahydroquinolines as potential anti-cancer agents.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 5, p. 853, doi. 10.3109/14756366.2015.1064120
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- Article
Structural, Optical Properties, and Biological Activity of Complexes Based on Derivatives of Quinoline, Quinoxaline, and Quinazoline with Metal Centers from Across the Periodic Table.
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- Comments on Inorganic Chemistry, 2014, v. 34, n. 5-6, p. 142, doi. 10.1080/02603594.2014.959116
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Determination of Antioxidant Capacity of 2,6-Quinolinediol.
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- Journal of the Institute of Science & Technology / Iğdır Üniversitesi Fen Bilimleri Enstitüsü Dergisi, 2019, v. 9, n. 3, p. 1520, doi. 10.21597/jist.553129
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Quinoline, with the active site of 8‐hydroxyl, efficiently inhibits Micropterus salmoides rhabdovirus (MSRV) infection in vitro and in vivo.
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- Journal of Fish Diseases, 2022, v. 45, n. 6, p. 895, doi. 10.1111/jfd.13615
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- Article
Simple quinoline-based 'turn-on' fluorescent sensor for imaging copper (II) in living cells.
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- Canadian Journal of Chemistry, 2014, v. 92, n. 11, p. 1092, doi. 10.1139/cjc-2014-0011
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A Computational Study of Quinoline Derivatives as Corrosion Inhibitors for Mild Steel in Acidic Medium.
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- Journal of Applied Sciences & Environmental Management, 2019, v. 23, n. 10, p. 1819, doi. 10.4314/jasem.v23i10.8
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- Article
Investigating the Anti-inflammatory Effect of Quinoline Derivative: N1-(5-methyl-5H-indolo[2,3-b]quinolin-11-yl)benzene-1,4-diamine Hydrochloride Loaded Soluble Starch Nanoparticles Against Methotrexate-induced Inflammation in Experimental Model.
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- Biological Procedures Online, 2024, v. 26, n. 1, p. 1, doi. 10.1186/s12575-024-00240-7
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- Article
Preparation of Novel Chitosan Oligosaccharide Quaternary Ammonium Derivatives Bearing Quinoline with Antioxidative and Antibacterial Activities.
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- Starch / Staerke, 2023, v. 75, n. 9/10, p. 1, doi. 10.1002/star.202300001
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HPLC‐ECD and TDDFT‐ECD study of hexahydropyrrolo[1,2‐a]quinoline derivatives.
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- Chirality, 2018, v. 30, n. 7, p. 866, doi. 10.1002/chir.22969
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