Works about PHTHALAZINE
Results: 217
Visible‐Light‐Promoted Cascade Coupling of 2‐Isocyanonaphthalenes with Elemental Sulfur and Amines to Construct Naphtho[2,1‐d]thiazol‐2‐Amines.
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- Chemistry - A European Journal, 2024, v. 30, n. 27, p. 1, doi. 10.1002/chem.202400719
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Shedding Light on the Diverse Reactivity of NacNacAl with N‐Heterocycles.
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- Angewandte Chemie, 2020, v. 132, n. 37, p. 16281, doi. 10.1002/ange.202005925
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Straightforward Synthesis and Properties of Highly Fluorescent [5]‐ and [7]‐Helical Dispiroindeno[2,1‐c]fluorenes.
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- Angewandte Chemie, 2019, v. 131, n. 48, p. 17329, doi. 10.1002/ange.201908348
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Molecular and crystal structure of iron(III) and nickel(II) complexes with 1′-phthalazinylhydrazones of heterocyclic carbonyl compounds.
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- Journal of Structural Chemistry, 2015, v. 56, n. 1, p. 102, doi. 10.1134/S002247661501014X
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Crystal structure of a trinuclear complex of zinc(II) with 2,6-Di- tert-butyl- p-quinone 1′-phthalazinylhydrazone.
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- Journal of Structural Chemistry, 2014, v. 55, n. 3, p. 475, doi. 10.1134/S0022476614030123
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Synthesis of fused dihydrobenzo [4,5]imidazo[1,2- a]pyrmido[5,4-e]pyrmidin-3(4H)-amine derivatives.
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- Al-Qadisiyah Journal of Pure Science, 2021, v. 26, n. 4, p. 34, doi. 10.29350/qjps.2021.26.4.1371
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SYNTHESIS, CHARACTERIZATION AND STUDY BIOLOGICAL ACTIVITY SOME NEW DERIVATIVES AMIDE AND PYRAZOLE -PYRAZOLINE OF STEROID ANALOGS.
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- Al-Qadisiyah Journal of Pure Science, 2019, v. 24, n. 3, p. 37
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4,4'-trimethylenedipiperidine as a nitrogen heterocycle solvent and/or catalyst: Liquid phase tandem Knoevenagel--Michael condensation.
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- Turkish Journal of Chemistry, 2021, v. 45, n. 1, p. 261, doi. 10.3906/kim-2010-41
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Topo II inhibition and DNA intercalation by new phthalazine-based derivatives as potent anticancer agents: design, synthesis, anti-proliferative, docking, and in vivo studies.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2022, v. 37, n. 1, p. 299, doi. 10.1080/14756366.2021.2007905
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Design and synthesis of phthalazine-based compounds as potent anticancer agents with potential antiangiogenic activity via VEGFR-2 inhibition.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2019, v. 34, n. 1, p. 1347, doi. 10.1080/14756366.2019.1642883
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Synthesis and blood glucose lowering activity of some novel benzenesulfonylthiourea derivatives substituted with 4-aryl-1-oxophthalazin-2(1H)yl-ones.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2014, v. 29, n. 3, p. 362, doi. 10.3109/14756366.2013.782300
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Synthesis and anticonvulsant activity evaluation of 6-substituted-[1,2,4]triazolo[3,4-a](tetrazolo[5,1-a])phthalazine derivatives.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2013, v. 28, n. 4, p. 792, doi. 10.3109/14756366.2012.684052
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Phyto-Biochemical Constituents and GC-MS Analysis of Bidens Pilosa Leaves and Stems.
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- Egyptian Academic Journal of Biological Sciences, H. Botany, 2022, v. 13, n. 2, p. 1, doi. 10.21608/EAJBSH.2022.247472
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Tetrahydrophthalazine Derivative »Sodium Nucleinate« Exert its Anti-Inflammatory Effects through Inhibition of Oxidative Burst in Human Monocytes.
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- Collegium Antropologicum, 2012, v. 36, n. 2, p. 409
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A Tetrahydrophthalazine Derivative »Sodium Nucleinate« Exerts a Potent Suppressive Effect upon LPS-Stimulated Mononuclear Cells in vitro and in vivo.
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- Collegium Antropologicum, 2011, v. 35, n. 4, p. 1219
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One-Pot Synthesis of Substituted Phthalazine-5,10-dione Derivatives in the Presence of Triflate Catalyst.
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- Journal of the Institute of Science & Technology / Iğdır Üniversitesi Fen Bilimleri Enstitüsü Dergisi, 2019, v. 9, n. 1, p. 468, doi. 10.21597/jist.433331
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Tel-Cu-NPs Catalyst: Synthesis of Naphtho[2,3- g ]phthalazine Derivatives as Potential Inhibiters of Tyrosinase Enzymes and Their Investigation in Kinetic, Molecular Docking, and Cytotoxicity Studies.
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- Catalysts (2073-4344), 2020, v. 10, n. 12, p. 1442, doi. 10.3390/catal10121442
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N‐substituted phthalazine sulfonamide derivatives as non‐classical aldose reductase inhibitors.
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- Journal of Molecular Recognition, 2022, v. 35, n. 12, p. 1, doi. 10.1002/jmr.2991
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Synthesis of hydrazine and azapeptide derivatives by alkylation of carbazates and semicarbazones.
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- Canadian Journal of Chemistry, 2012, v. 90, n. 11, p. 985, doi. 10.1139/v2012-070
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A DFT study on the mechanism and selectivity of [3 + 2] cycloaddition reactions leading to pyrole[2,1-a] phthalazine compounds.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2021, v. 140, n. 5, p. 1, doi. 10.1007/s00214-021-02756-7
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DINUCLEAR SILVER(I) COMPLEXES WITH PHTHALAZINE: DNA/BSA BINDING AND IN VIVO TOXICITY STUDY.
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- Kragujevac Journal of Science, 2023, v. 45, p. 79, doi. 10.5937/KgJSci2345079A
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A NOVEL, GREEN AND HETEROGENEOUS CERIA-BASED SOLID LEWIS ACID CATALYST ASSISTED ONE-POT MULTICOMPONENT SYNTHESIS OF DIHYDROPYRANO[ 2,3-C]PYRAZOLES.
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- Rasayan Journal of Chemistry, 2021, v. 14, n. 2, p. 1415, doi. 10.31788/RJC.2021.1426069
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ONE POT SYNTHESIS OF PYRAZOLO PHTHALAZINE DIONE DERIVATIVES UNDER MICROWAVE IRRADIATION.
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- Rasayan Journal of Chemistry, 2019, v. 12, n. 2, p. 415, doi. 10.31788/RJC.2019.1225035
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Nano-pistachio hull-OxTiCl4 − x: synthesis, characterization and application as an effective and novel nanocatalyst for one-pot synthesis of dihydropyrano[3,2-b]chromenedione derivatives.
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- Journal of the Iranian Chemical Society, 2021, v. 18, n. 5, p. 1137, doi. 10.1007/s13738-020-02096-6
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CuO nanoparticles as a reusable catalyst for the synthesis of 1H-pyrazolo[1,2-b]phthalazine-5,10-dione derivatives under solvent-free conditions.
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- Journal of the Iranian Chemical Society, 2019, v. 16, n. 8, p. 1665, doi. 10.1007/s13738-019-01640-3
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Design and development of a new functionalized cellulose-based magnetic nanocomposite: preparation, characterization, and catalytic application in the synthesis of diverse pyrano[2,3-c]pyrazole derivatives.
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- Journal of the Iranian Chemical Society, 2019, v. 16, n. 7, p. 1459, doi. 10.1007/s13738-019-01610-9
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Synthesis of novel spiro[chromeno[4′,3′:3,4]pyrazolo[1,2-b]phthalazine-7,3′-indoline]-2′,6,9,14-tetraone.
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- Journal of the Iranian Chemical Society, 2019, v. 16, n. 2, p. 263, doi. 10.1007/s13738-018-1506-9
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A new simple method for the preparation of PbO nanoparticles and implementation of an efficient and reusable catalytic system for the synthesis of 1 H-pyrazolo[1,2-b]phthalazine-5,10-diones.
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- Journal of the Iranian Chemical Society, 2017, v. 14, n. 6, p. 1179, doi. 10.1007/s13738-017-1068-2
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Urea-functionalized silica-coated FeTiO magnetic nanoparticles: as highly efficient and recyclable heterogeneous nanocatalyst for synthesis of 4 H-chromene and 1 H-pyrazolo[1,2-b]phthalazine-5,10-dione derivatives.
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- Journal of the Iranian Chemical Society, 2017, v. 14, n. 2, p. 403, doi. 10.1007/s13738-016-0989-5
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Saccharin: a green, economical and efficient catalyst for the one-pot, multi-component synthesis of 3,4-dihydropyrimidin-2-(1 H)-one derivatives and 1 H-pyrazolo [1,2- b] phthalazine-5,10-dione derivatives and substituted dihydro-2-oxypyrrole.
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- Journal of the Iranian Chemical Society, 2016, v. 13, n. 6, p. 1549, doi. 10.1007/s13738-016-0871-5
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Ultrasound-assisted multi-component synthesis of indazolophthalazine derivatives.
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- Journal of the Iranian Chemical Society, 2015, v. 12, n. 9, p. 1613, doi. 10.1007/s13738-015-0634-8
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Application of citric acid as highly efficient and green organocatalyst for multi-component synthesis of indazolo[2,1- b]phthalazine-triones.
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- Journal of the Iranian Chemical Society, 2013, v. 10, n. 3, p. 577, doi. 10.1007/s13738-012-0193-1
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Nano-ZnO: an efficient and reusable catalyst for one-pot synthesis of 1H-pyrazolo[1,2-b]phthalazine-5,10-diones and pyrazolo[1,2-a][1,2,4]triazole-1,3-diones.
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- Journal of the Iranian Chemical Society, 2013, v. 10, n. 2, p. 297, doi. 10.1007/s13738-012-0159-3
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Synthesis of phthalazine-based derivatives as selective anti-breast cancer agents through EGFR-mediated apoptosis: in vitro and in silico studies.
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- BMC Chemistry, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s13065-023-00995-2
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Synthesis and antimicrobial evaluation of some annelated phthalazine derivatives and acyclo C-nucleosides from 1-chloro-4-(2,4,6-trimethylphenyl) phthalazine precursor.
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- Turkish Journal of Chemistry, 2012, v. 36, n. 3, p. 347, doi. 10.3906/kim-1111-52
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Iron Catalyzed [3+2] Cycloaddition of Tetrahydroisoquinoline: Synthesis of Dihydropyrrolo[2,1‐a]isoquinolines.
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- Asian Journal of Organic Chemistry, 2020, v. 9, n. 10, p. 1617, doi. 10.1002/ajoc.202000211
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Catalyst free sequential one‐pot reaction for the synthesis of 3‐indole propanoates/propanoic acid/propanamides as antituberculosis agents.
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- Journal of the Chinese Chemical Society, 2021, v. 68, n. 1, p. 39, doi. 10.1002/jccs.202000386
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Synthesis, anti‐inflammatory activity, and molecular docking study of novel azo bis antipyrine derivatives against cyclooxygenase‐2 enzyme.
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- Journal of the Chinese Chemical Society, 2021, v. 68, n. 1, p. 27, doi. 10.1002/jccs.202000265
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Synthesis, anticancer evaluation, and docking studies of some novel azo chromene derivatives.
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- Journal of the Chinese Chemical Society, 2020, v. 67, n. 10, p. 1877, doi. 10.1002/jccs.201900481
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Fe<sub>3</sub>O<sub>4</sub>@SiO<sub>2</sub>@sulfated boric acid as superparamagnetic and recyclable nanocatalyst‐assisted, one‐pot, pseudo four‐component synthesis of 5‐amino‐2‐aryl‐3H‐chromeno[4,3,2‐de][1,6]naphthyridine‐4‐carbonitrile derivatives
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- Journal of the Chinese Chemical Society, 2019, v. 66, n. 12, p. 1641, doi. 10.1002/jccs.201900044
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A one‐pot green synthesis of 2‐amino‐4H‐benzo[h]chromenes catalyzed by a dioxomolybdenum Schiff base complex supported on magnetic nanoparticles as an efficient and recyclable nanocatalyst.
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- Journal of the Chinese Chemical Society, 2019, v. 66, n. 7, p. 775, doi. 10.1002/jccs.201800149
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Facile synthesis of multi‐functional 1,3,4‐thiadiazine derivatives bearing phthalazine, pyridazine, and pyrido‐pyridazine moieties.
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- Journal of the Chinese Chemical Society, 2019, v. 66, n. 2, p. 231, doi. 10.1002/jccs.201800093
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Stereoselective Synthesis of Pyrrolo/Pyrido[2,1‐a]isoindoles via Alkyne Iminium Ion Cyclization of Vinylogous Carbamates.
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- Chemistry - An Asian Journal, 2023, v. 18, n. 19, p. 1, doi. 10.1002/asia.202300626
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Montmorillonite K-10 Supported 11-molybdo-1-vanadophosphoric Acid (H<sub>4</sub>PMo<sub>11</sub>V<sub>1</sub>O<sub>40</sub>/K-10) Catalysts for Environmentally Benign Synthesis of 2H-indazolo[2,1-b]phthalazine-triones Under Solvent-free Condition.
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- Orbital: The Electronic Journal of Chemistry, 2017, v. 9, n. 4, p. 210, doi. 10.17807/orbital.v9i4.873
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Synthesis of naphtho- and pyrazolo-fused systems by an intramolecular Friedel--Crafts approach.
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- Australian Journal of Chemistry, 2023, v. 76, n. 11, p. 760, doi. 10.1071/CH23030
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Mechanistic Studies on the Bidentate Lewis Acid Catalyzed Domino Inverse Electron‐Demand Diels‐Alder/Thiol Transfer Reaction.
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- European Journal of Organic Chemistry, 2023, v. 26, n. 8, p. 1, doi. 10.1002/ejoc.202201289
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A Enamide‐Based Diastereoselective Synthesis of Isoindolo[2,1‐a]quinolin‐11(5H)‐ones with Three Contiguous Stereogenic Centers.
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- European Journal of Organic Chemistry, 2023, v. 26, n. 5, p. 1, doi. 10.1002/ejoc.202201318
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Ruthenium(II)‐Catalyzed Annulation of 2‐Arylimidazoles with Arylglyoxals: Synthesis of 5‐Hydroxyimidazo[2,1‐a]isoquinolin‐6(5H)‐ones and Their Photophysical Studies.
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- European Journal of Organic Chemistry, 2023, v. 26, n. 1, p. 1, doi. 10.1002/ejoc.202201065
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Effect of commonly used organic solvents on Aldehyde oxidase-mediated Vanillin, Phthalazine and Methotrexate oxidation in human, rat and mouse liver subcellular fractions.
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- Xenobiotica, 2014, v. 44, n. 8, p. 722, doi. 10.3109/00498254.2014.889332
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Identification of a suitable and selective inhibitor towards aldehyde oxidase catalyzed reactions.
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- Xenobiotica, 2014, v. 44, n. 3, p. 197, doi. 10.3109/00498254.2013.819594
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