Works matching DE "COUMARIN derivatives"
Results: 526
Synthesis and Study of Copolymers Bearing Two Coumarin Side Groups in Monomer Unit: Toward Photoalignment of Liquid Crystals.
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- Macromolecular Chemistry & Physics, 2023, v. 224, n. 19, p. 1, doi. 10.1002/macp.202300191
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Boron Compounds as Additives for the Cationic Polymerization Using Coumarin Derivatives in Epoxy Silicones.
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- Macromolecular Chemistry & Physics, 2021, v. 222, n. 2, p. 1, doi. 10.1002/macp.202000404
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Rational Design of Coumarin‐Based Hybridized Local and Charge‐Transfer Blue Emitters for Solution‐Processed Organic Light‐Emitting Diodes.
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- Chemistry - A European Journal, 2024, v. 30, n. 39, p. 1, doi. 10.1002/chem.202401078
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Two New Coumarins with Immunomodulatory and Anticancer Activities from Sterculia colorata.
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- Chemistry of Natural Compounds, 2023, v. 59, n. 3, p. 436, doi. 10.1007/s10600-023-04018-3
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Coumarin-Xanthone Derivatives with Hepatoprotective Activities from Pyrethrum tatsienense.
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- Chemistry of Natural Compounds, 2023, v. 59, n. 1, p. 36, doi. 10.1007/s10600-023-03912-0
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New Coumarin and Bioactive Constituents of Chionanthus retusus.
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- Chemistry of Natural Compounds, 2021, v. 57, n. 5, p. 835, doi. 10.1007/s10600-021-03492-x
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4-Methyl-7-Amino/Amido Coumarin Derivatives as Potential Antimicrobials and Antioxidants.
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- Chemistry of Natural Compounds, 2020, v. 56, n. 4, p. 614, doi. 10.1007/s10600-020-03106-y
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Fatty Acids and Coumarins of <italic>Fraxinus syriaca</italic>.
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- Chemistry of Natural Compounds, 2018, v. 54, n. 1, p. 166, doi. 10.1007/s10600-018-2284-4
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Modified Coumarins. 36. Synthesis of Linear and Angular Dihydropyranocoumarincarboxylic Acids.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 3, p. 399, doi. 10.1007/s10600-016-1658-8
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Modified Coumarins. 33. Synthesis of Furo- and Dihydropyranocoumarins Containing a Lupinine Moiety.
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- Chemistry of Natural Compounds, 2015, v. 51, n. 5, p. 815, doi. 10.1007/s10600-015-1423-4
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DNA Origami Steganography Based on Photocleavable Oligonucleotides.
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- ChemPhotoChem, 2024, v. 8, n. 10, p. 1, doi. 10.1002/cptc.202400132
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Coumarin-based fluorescent sensors for zinc(II) and hypochlorite.
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- Supramolecular Chemistry, 2015, v. 27, n. 11/12, p. 798, doi. 10.1080/10610278.2015.1077958
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Coumarin Triazoles as Potential Antimicrobial Agents.
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- Antibiotics (2079-6382), 2023, v. 12, n. 1, p. 160, doi. 10.3390/antibiotics12010160
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Molecular Insights into Coumarin Analogues as Antimicrobial Agents: Recent Developments in Drug Discovery.
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- Antibiotics (2079-6382), 2022, v. 11, n. 5, p. 566, doi. 10.3390/antibiotics11050566
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Determining the 3-substituted Coumarins inhibitory potential against the HslV protease of E. coli.
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- European Review for Medical & Pharmacological Sciences, 2023, v. 27, n. 19, p. 9169
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THE PROTECTIVE ROLE OF NATURAL COUMARINS DERIVATIVES AND ANPRO SUPPLEMENT AGAINST AFLATOXIN B1 POLLUTION IN THE QUAILS COTURNIX JAPONICA DIET.
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- Mesopotamia Journal of Agriculture, 2023, v. 51, n. 1, p. 1, doi. 10.33899/magrj.2023.136713.1205
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Microwave-Assisted Synthesis of Substituted 2-(2H-Chromen-3-yl)-5-phenyl-1H-imidazole Based Coumarin Derivatives and Their Antimicrobial Activity.
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- Russian Journal of General Chemistry, 2021, v. 91, n. 4, p. 711, doi. 10.1134/S1070363221040216
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A new strategy for synthesis of 9-benzoyl-4-methylpyrano[2,3- f]chromene-2,8-dione using L-proline as a novel and efficient catalyst.
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- Russian Journal of General Chemistry, 2016, v. 86, n. 12, p. 2732, doi. 10.1134/S1070363216120331
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Exploring the dynamics of halogen and hydrogen bonds in halogenated coumarins.
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- Zeitschrift für Physikalische Chemie, 2024, v. 238, n. 9, p. 1731, doi. 10.1515/zpch-2023-0570
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New Pd(II) complexes containing hydrazinyl oxazolyl coumarin derivatives: synthesis, spectral characterization and anti-cancer studies.
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- Zeitschrift für Physikalische Chemie, 2024, v. 238, n. 2, p. 261, doi. 10.1515/zpch-2023-0380
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Continuous Flow Biocatalysis: Synthesis of Coumarin Carboxamide Derivatives by Lipase TL IM from Thermomyces lanuginosus.
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- Catalysts (2073-4344), 2022, v. 12, n. 3, p. 339, doi. 10.3390/catal12030339
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Copper-Catalyzed Synthesis of Coumarins. A Mini-Review.
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- Catalysts (2073-4344), 2021, v. 11, n. 11, p. 1382, doi. 10.3390/catal11111382
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NMR-Based Metabolomics to Analyze the Effects of a Series of Monoamine Oxidases-B Inhibitors on U251 Cells.
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- Biomolecules (2218-273X), 2023, v. 13, n. 4, p. 600, doi. 10.3390/biom13040600
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Development of New Multicomponent Reactions in Eco-Friendly Media-Greener Reaction and Expeditious Synthesis of Novel Bioactive Benzylpyranocoumarins.
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- Journal of Chemistry, 2019, p. 1, doi. 10.1155/2019/8693614
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Synthesis of Novel 1,2,4-Triazolyl Coumarin Derivatives as Potential Anticancer Agents.
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- Journal of Chemistry, 2018, p. 1, doi. 10.1155/2018/5201374
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SYNTHESIS, CHARACTERIZATION AND ANTIBACTERIAL ACTIVITIES OF NEWLY SYNTHESIZED COUMARIN DERIVATIVES.
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- International Journal of Pharmaceutical, Chemical & Biological Sciences, 2017, v. 7, n. 4, p. 352
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Biogenic CuO NPs for synthesis of coumarin derivatives in hydrotropic aqueous medium.
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- Research on Chemical Intermediates, 2023, v. 49, n. 7, p. 2989, doi. 10.1007/s11164-023-05034-2
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Supported palladium oxide nanoparticles in Al-SBA-15 as an efficient and reusable catalyst for the synthesis of pyranopyrazole and benzylpyrazolyl coumarin derivatives via multicomponent reactions.
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- Research on Chemical Intermediates, 2022, v. 48, n. 1, p. 203, doi. 10.1007/s11164-021-04619-z
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Pharmacological Evaluation and Docking Studies of 3-Thiadiazolyl- and Thioxo-1,2,4-triazolylcoumarin Derivatives as Cholinesterase Inhibitors.
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- ISRN Pharmacology, 2012, p. 1, doi. 10.5402/2012/707932
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BIOLOGICAL ACTIVITIES OF EXTRACTS AND SECONDARY METABOLITE OF Macaranga mappa BARK AS AN ANTIDIABETIC BY a-GLUCOSIDASE INHIBITOR, ANTIOXIDANT, AND CYTOTOXICITY.
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- Rasayan Journal of Chemistry, 2023, v. 16, n. 1, p. 290, doi. 10.31788/RJC.2023.1618029
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CAMBRIDGE STRUCTURE DATABASE ANALYSIS OF MOLECULAR INTERACTION ENERGIES IN BROMINE-SUBSTITUTED COUMARIN STRUCTURES.
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- Rasayan Journal of Chemistry, 2022, v. 15, n. 2, p. 991, doi. 10.31788/RJC.2022.1526853
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5-SULFOSALICYLIC ACID (5-SSA): AN EFFICIENT ORGANOCATALYST FOR THE SYNTHESIS OF 4-METHYLCOUMARINS VIA PECHMANN CONDENSATION.
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- Rasayan Journal of Chemistry, 2020, v. 13, n. 4, p. 2466, doi. 10.31788/RJC.2020.1345950
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MULTICOMPONENT REACTIONS OF CYANOACETANILIDE DERIVATIVES: SYNTHESIS OF COUMARIN AND QUINOLINE DERIVATIVE AND EVALUATIONS OF THEIR CYTOTOXICITY.
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- Bulletin of the Chemical Society of Ethiopia, 2024, v. 38, n. 3, p. 739, doi. 10.4314/bcse.v38i3.15
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DESIGN, SYNTHESIS, AND CYTOTOXIC ACTIVITY OF SOME NOVEL N-(SUBSTITUTED) BENZAMIDE DERIVATIVES BEARING COUMARIN AND 1-AZOCOUMARIN COMPOUNDS.
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- Bulletin of the Chemical Society of Ethiopia, 2023, v. 37, n. 4, p. 1003, doi. 10.4314/bcse.v37i4.16
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THE USES OF ETHYL 2-(1H-BENZO[D]IMIDAZOL-2-YL)ACETATE TO SYNTHESIS PYRAZOLE, THIOPHENE, PYRIDINE AND COUMARIN DERIVATIVES WITH ANTITUMOR ACTIVITIES.
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- Bulletin of the Chemical Society of Ethiopia, 2018, v. 32, n. 3, p. 541, doi. 10.4314/bcse.v32i3.13
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Cytotoxic Properties of Three Isolated Coumarin-hemiterpene Ether Derivatives from Artemisia armeniaca Lam.
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- Iranian Journal of Pharmaceutical Research, 2017, v. 16, n. 1, p. 221
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Evaluation of the Anti-diabetic Activity of Purified Compounds of Ferula assafoetida by in vitro and in silico Methods.
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- Natural Product Communications, 2024, v. 19, n. 6, p. 1, doi. 10.1177/1934578X241257125
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Chemical Constituents Isolated from the Leaves of Toricellia angulata Oliv. var. intermedia (Harms.) Hu.
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- Natural Product Communications, 2021, v. 16, n. 10, p. 1, doi. 10.1177/1934578X211045464
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Microwave-promoted Synthesis of Novel Fused Osthole Analogues.
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- Chinese Journal of Chemistry, 2016, v. 34, n. 12, p. 1344, doi. 10.1002/cjoc.201600489
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Synthesis of Osthole Derivatives with Grignard Reagents and Their Larvicidal Activities on Mosquitoes.
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- Chinese Journal of Chemistry, 2015, v. 33, n. 12, p. 1353, doi. 10.1002/cjoc.201500620
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Manganese(III) Salen Complex Immobilized on Fe<sub>3</sub>O<sub>4</sub> Magnetic Nanoparticles: The Efficient, Green and Reusable Nanocatalyst.
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- Chinese Journal of Chemistry, 2014, v. 32, n. 4, p. 349, doi. 10.1002/cjoc.201400007
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A QSAR Study for the Prediction of Inhibitory Activity of Coumarin Derivatives for the Treatment of Alzheimer's Disease.
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- Arabian Journal for Science & Engineering (Springer Science & Business Media B.V. ), 2021, v. 46, n. 6, p. 5523, doi. 10.1007/s13369-020-05064-7
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Coumarin derivatives as new anti-biofilm agents against Staphylococcus aureus.
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- PLoS ONE, 2024, v. 19, n. 9, p. 1, doi. 10.1371/journal.pone.0307439
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Europium activated bismuth containing double perovskite catalyzed synthesis of coumarin derivatives and its cytotoxicity evaluation.
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- Journal of the Iranian Chemical Society, 2025, v. 22, n. 2, p. 445, doi. 10.1007/s13738-024-03161-0
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Synthesis and biological evaluation of novel coumarin derivatives bearing sulfonamide moiety as potent α-glucosidase inhibitors.
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- Journal of the Iranian Chemical Society, 2025, v. 22, n. 1, p. 207, doi. 10.1007/s13738-024-03143-2
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Synthesis, characterization, antimicrobial activity and molecular docking study of transition metal complexes based on azo coumarin and thiosemicarbazone derivative.
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- Journal of the Iranian Chemical Society, 2024, v. 21, n. 3, p. 719, doi. 10.1007/s13738-023-02953-0
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High-sensitivity dual-channel chemical sensor based on carboxylic acid-functionalized coumarin derivative for detecting CN<sup>−</sup> in aqueous medium.
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- Journal of the Iranian Chemical Society, 2021, v. 18, n. 11, p. 3137, doi. 10.1007/s13738-021-02258-0
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One-pot electrochemical synthesis of highly symmetric and conjugated coumarin derivative.
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- Journal of the Iranian Chemical Society, 2018, v. 15, n. 12, p. 2669, doi. 10.1007/s13738-018-1455-3
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One-pot synthesis, spectroscopic characterization and DFT study of novel 8-azacoumarin derivatives as eco-friendly insecticidal agents.
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- Journal of the Iranian Chemical Society, 2018, v. 15, n. 9, p. 2093, doi. 10.1007/s13738-018-1402-3
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The synthesis of coumarin derivatives using choline chloride/zinc chloride as a deep eutectic solvent.
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- Journal of the Iranian Chemical Society, 2016, v. 13, n. 1, p. 149, doi. 10.1007/s13738-015-0722-9
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