Works matching DE "QUINOXALINES"
Results: 815
Crystal structure of 9-chloro-2,3,4,4a,5,6-hexahydro-1H-pyrido [1′,2′:1,6]pyrazino[2,3-b]quinoxaline, C<sub>14</sub>H<sub>15</sub>ClN<sub>4</sub>.
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- Zeitschrift für Kristallographie / New Crystal Structures, 2025, v. 240, n. 2, p. 207, doi. 10.1515/ncrs-2024-0422
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Synthesis of a Multifunctional Quinoxaline and Benzodithiophene Bearing Polymer and Its Electrochromic Device Applications.
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- Macromolecular Chemistry & Physics, 2020, v. 221, n. 6, p. 1, doi. 10.1002/macp.201900470
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Synthesis of Alkyl‐Substituted Quinoxaline‐Based Copolymers Along with Photophysical Property Modulation for Polymer Solar Cells.
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- Macromolecular Chemistry & Physics, 2018, v. 219, n. 15, p. 1, doi. 10.1002/macp.201800117
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Cover Feature: Transition Behaviors of Isostructural Hydrogen‐Bonded Frameworks Composed of Naphthalene, Quinoxaline, and Pyrazinopyrazine Derivatives (Chem. Eur. J. 44/2024).
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- Chemistry - A European Journal, 2024, v. 30, n. 44, p. 1, doi. 10.1002/chem.202484404
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Photo‐Induced Generation of Oxygenated Quaternary Centers via EnT Enabled Singlet O<sub>2</sub> Addition to C3‐Maleimidated Quinoxaline: A Reagent‐Less Approach.
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- Chemistry - A European Journal, 2024, v. 30, n. 45, p. 1, doi. 10.1002/chem.202400219
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Modulating Strain in Twisted Pyrene‐Fused Azaacenes.
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- Chemistry - A European Journal, 2023, v. 29, n. 69, p. 1, doi. 10.1002/chem.202302002
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Theoretical Prediction of Electrocatalytic Reduction of CO<sub>2</sub> Using a 2D Catalyst Composed of 3 d Transition Metal and Hexaamine Dipyrazino Quinoxaline.
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- Chemistry - A European Journal, 2023, v. 29, n. 64, p. 1, doi. 10.1002/chem.202302232
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Cover Feature: Substrate‐Controlled Product Divergence in Iron(III)‐Catalyzed Reactions of Propargylic Alcohols: Easy Access to Spiro‐indenyl 1,4‐Benzoxazines and 2‐(2,2‐Diarylvinyl)quinoxalines (Chem. Eur. J. 13/2023).
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- Chemistry - A European Journal, 2023, v. 29, n. 13, p. 1, doi. 10.1002/chem.202203993
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Substrate‐Controlled Product Divergence in Iron(III)‐Catalyzed Reactions of Propargylic Alcohols: Easy Access to Spiro‐indenyl 1,4‐Benzoxazines and 2‐(2,2‐Diarylvinyl)quinoxalines.
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- Chemistry - A European Journal, 2023, v. 29, n. 13, p. 1, doi. 10.1002/chem.202203993
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Metal–ligand Lability and Ligand Mobility Enables Framework Transformation via Ligand Release in a Family of Crystalline 2D Coordination Polymers.
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- Chemistry - A European Journal, 2022, v. 28, n. 51, p. 1, doi. 10.1002/chem.202201408
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Synthesis of N‐Heterocycles via Oxidant‐Free Dehydrocyclization of Alcohols Using Heterogeneous Catalysts.
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- Angewandte Chemie, 2021, v. 133, n. 48, p. 25392, doi. 10.1002/ange.202104979
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Exporting Metal‐Carbene Chemistry to Live Mammalian Cells: Copper‐Catalyzed Intracellular Synthesis of Quinoxalines Enabled by N−H Carbene Insertions.
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- Angewandte Chemie, 2021, v. 133, n. 40, p. 22188, doi. 10.1002/ange.202108899
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(Aza)Acenes Share the C2 Bridge with (Anti)Aromatic Macrocycles: Local vs. Global Delocalization Paths.
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- Angewandte Chemie, 2021, v. 133, n. 16, p. 9145, doi. 10.1002/ange.202011848
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Copper(I)‐Catalyzed Asymmetric Vinylogous Aldol‐Type Reaction of Allylazaarenes.
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- Angewandte Chemie, 2021, v. 133, n. 9, p. 4654, doi. 10.1002/ange.202013207
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A Coplanar π‐Extended Quinoxaline Based Hole‐Transporting Material Enabling over 21 % Efficiency for Dopant‐Free Perovskite Solar Cells.
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- Angewandte Chemie, 2021, v. 133, n. 5, p. 2706, doi. 10.1002/ange.202013128
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Photophysics of Molecular-Weight-Induced Losses in Indacenodithienothiophene-Based Solar Cells.
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- Advanced Functional Materials, 2015, v. 25, n. 30, p. 4898, doi. 10.1002/adfm.201501062
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Deep Cavitand Self-Assembled on Au NPs-MWCNT as Highly Sensitive Benzene Sensing Interface.
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- Advanced Functional Materials, 2015, v. 25, n. 26, p. 4011, doi. 10.1002/adfm.201501234
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Origin of Reduced Bimolecular Recombination in Blends of Conjugated Polymers and Fullerenes.
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- Advanced Functional Materials, 2014, v. 23, n. 34, p. 4262, doi. 10.1002/adfm.201203852
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Synthesis of Quinoxaline Derivatives as Intermediates to Obtain Erdafitinib.
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- Pharmaceutical Chemistry Journal, 2021, v. 55, n. 9, p. 951, doi. 10.1007/s11094-021-02521-x
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Synthesis and Cytotoxic Activity of Fluorine-Containing 6,7-Dihydroindazolone and 6,7-Dihydrobenzisoxazolone Derivatives.
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- Pharmaceutical Chemistry Journal, 2020, v. 54, n. 7, p. 700, doi. 10.1007/s11094-020-02258-z
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Synthesis and Biological Activity of 2,3-Bis-(2-Oxoylidene)-1,2,3,4-Tetrahydroquinoxalines.
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- Pharmaceutical Chemistry Journal, 2015, v. 48, n. 10, p. 640, doi. 10.1007/s11094-015-1163-6
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New Opportunities for the Synthesis of Quinoxaline-Substituted Heterocyclic and Aryl Moieties.
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- Pharmaceutical Chemistry Journal, 2013, v. 47, n. 9, p. 498, doi. 10.1007/s11094-013-0989-z
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A simple means of preparing quinoxaline derivatives: direct introduction of C-nucleophiles into the quinoxaline nucleus by substituting a hydrogen atom.
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- Pharmaceutical Chemistry Journal, 2013, v. 47, n. 3, p. 172, doi. 10.1007/s11094-013-0919-0
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Synthesis and analgesic activity of the products of the interaction between 3-aroylpyrrolo[1,2- a]-quinoxaline-1,2,4(5 H)-triones with benzoic acid hydrazides.
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- Pharmaceutical Chemistry Journal, 2012, v. 45, n. 11, p. 660, doi. 10.1007/s11094-012-0697-0
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Synthesis and antimicrobial activity of substituted benzoxazines and quinoxalines.
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- Pharmaceutical Chemistry Journal, 2006, v. 40, n. 11, p. 611, doi. 10.1007/s11094-006-0204-6
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Structure and Optical Properties of Plane-Type And Z-Type Topology Triazole Quinoxaline Cd(II) Complexes.
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- Journal of Structural Chemistry, 2018, v. 59, n. 4, p. 922, doi. 10.1134/S002247661804025X
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Application of the AMYR calculating method on quinoxaline, 3-chloroquinoxaline, and 3-methylquinoxaline in the interaction with n water molecules ( n varies from 1 to 6).
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- Journal of Structural Chemistry, 2014, v. 55, n. 1, p. 38, doi. 10.1134/S0022476614010065
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Antibiotic residues in non-targeted animal feed – development of a sensitive LC-MS/MS methodology.
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- Veterinarska Stanica, 2025, v. 56, n. 2, p. 177, doi. 10.46419/vs.56.2.10
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MAOS of Quinoxalines, Conjugated Pyrazolylquinoxalines and Fused Pyrazoloquinoxalines from l-Ascorbic and d-Isoascorbic Acid.
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- Journal of Carbohydrate Chemistry, 2007, v. 26, n. 1, p. 1, doi. 10.1080/07328300701252359
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The critical role of oxidative stress in the toxicity and metabolism of quinoxaline 1,4-di- N -oxides in vitro and in vivo.
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- Drug Metabolism Reviews, 2016, v. 48, n. 2, p. 159, doi. 10.1080/03602532.2016.1189560
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Synthesis and photovoltaic characterization of triarylamine-substituted quinoxaline push--pull dyes to improve the performance of dye-sensitized solar cells.
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- Turkish Journal of Chemistry, 2017, v. 41, n. 3, p. 309, doi. 10.3906/kim-1603-15
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Synthesis and application of polyvinylimidazole-based Br0nsted acidic ionic liquid grafted silica as an efficient heterogeneous catalyst in the preparation of quinoxaline derivatives.
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- Turkish Journal of Chemistry, 2016, v. 40, n. 3, p. 422, doi. 10.3906/kim-1504-40
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New spiro-indeno[1,2-b]quinoxalines clubbed with benzimidazole scaffold as CDK2 inhibitors for halting non-small cell lung cancer; stereoselective synthesis, molecular dynamics and structural insights.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2023, v. 38, n. 1, p. 1, doi. 10.1080/14756366.2023.2281260
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Discovery of new VEGFR-2 inhibitors based on bis([1, 2, 4]triazolo)[4,3-a:3',4'-c]quinoxaline derivatives as anticancer agents and apoptosis inducers.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2021, v. 36, n. 1, p. 1093, doi. 10.1080/14756366.2021.1915303
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Quinoxalin-2-carboxamides: synthesis and pharmacological evaluation as serotonin type-3 (5-HT<sub>3</sub>) receptor antagonists.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2011, v. 26, n. 5, p. 610, doi. 10.3109/14756366.2010.543419
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Synthesis and antibacterial properties of new N<sub>4</sub>-acetylated hexahydro-2,7-dioxopyrido[2,3- f]quinoxaline-8-carboxylic acids.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2011, v. 26, n. 5, p. 649, doi. 10.3109/14756366.2010.543421
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Synthesis and evaluation of the antiproliferative activity of novel isoindolo[2,1- a]quinoxaline and indolo[1,2- a]quinoxaline derivatives.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2011, v. 26, n. 5, p. 657, doi. 10.3109/14756366.2010.548326
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A QSAR study on 2-(4-methylpiperazin-1-yl)quinoxalines as human histamine H<sub>4</sub> receptor ligands.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2011, v. 26, n. 3, p. 412, doi. 10.3109/14756366.2010.519702
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Design, synthesis, cytotoxic evaluation, and QSAR study of some 6H-indolo[2,3-b]quinoxaline derivatives.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2010, v. 25, n. 3, p. 394, doi. 10.3109/14756360903190747
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Pair wise binding affinity: 3D QSAR studies on a set of triazolo [1, 5-a] quinoxalines as antagonists of AMPA and KA receptors.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2009, v. 24, n. 4, p. 1008, doi. 10.1080/14756360802567979
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Synthesis of new 4-(E)-alkenylpyrrolo[1,2-a]quinoxalines as antileishmanial agents by Suzuki-Miyaura cross-coupling reactions.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2007, v. 22, n. 5, p. 541, doi. 10.1080/14756360701425089
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Quantitative structure-activity relationship study of human A3 adenosine receptor antagonists: Derivatives of 2-aryl-1,2,4-triazolo[4,3-α]quinoxaline.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2007, v. 22, n. 2, p. 165, doi. 10.1080/14756360601051290
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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 Quinoxalines and Their Two Main Metabolites in Environmental Water Samples by Liquid Chromatography–Tandem Mass Spectrometry.
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- Analytical Letters, 2014, v. 47, n. 8, p. 1421, doi. 10.1080/00032719.2013.867497
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Development of a Time-Resolved Fluoroimmunoassay for the Rapid Detection of Methyl-3-Quinoxaline-2-Carboxylic Acid in Porcine Tissues.
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- Analytical Letters, 2014, v. 47, n. 4, p. 606, doi. 10.1080/00032719.2013.845897
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Comparative Metabolism of Mequindox in Liver Microsomes, Hepatocytes, and Intestinal Microflora of Chicken.
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- Analytical Letters, 2012, v. 45, n. 13, p. 1749, doi. 10.1080/00032719.2012.677975
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Heterocyclic amines and genotype of N-acetyltransferases as risk factors for prostate cancer.
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- Prostate Cancer & Prostatic Diseases, 2005, v. 8, n. 1, p. 69, doi. 10.1038/sj.pcan.4500780
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The three pyridazines, three naphthyridines and two azoles: effect of the position of the second heteroatom on pK<sub>aH</sub> of their eight conjugate acids.
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- Zeitschrift für Physikalische Chemie, 2022, v. 236, n. 11/12, p. 1617, doi. 10.1515/zpch-2022-0111
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New 8-Hydroxyquinoline-Bearing Quinoxaline Derivatives as Effective Corrosion Inhibitors for Mild Steel in HCl: Electrochemical and Computational Investigations.
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- Coatings (2079-6412), 2020, v. 10, n. 9, p. 811, doi. 10.3390/coatings10090811
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Europium Nanoparticle-Based Lateral Flow Strip Biosensors for the Detection of Quinoxaline Antibiotics and Their Main Metabolites in Fish Feeds and Tissues.
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- Biosensors (2079-6374), 2024, v. 14, n. 6, p. 292, doi. 10.3390/bios14060292
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