Works matching DE "PYRIDINE derivatives"
Results: 847
The Co-Administration of Paclitaxel with Novel Pyridine and Benzofuran Derivatives that Inhibit Tubulin Polymerisation: A Promising Anticancer Strategy.
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- Pharmaceutics, 2025, v. 17, n. 2, p. 223, doi. 10.3390/pharmaceutics17020223
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Synthesis, Anticancer Screening, and In Silico Evaluations of Thieno[2,3- c ]pyridine Derivatives as Hsp90 Inhibitors.
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- Pharmaceuticals (14248247), 2025, v. 18, n. 2, p. 153, doi. 10.3390/ph18020153
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Microbial Enantioselective Reduction of Acetylpridine Derivatives.
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- Bioscience, Biotechnology & Biochemistry, 2003, v. 67, n. 4, p. 809, doi. 10.1271/bbb.67.809
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Functionalized Electron‐Rich Pyridines as Initiators for the Epoxy Homopolymerization.
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- Macromolecular Chemistry & Physics, 2024, v. 225, n. 2, p. 1, doi. 10.1002/macp.202300299
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Construction of Covalent Triazine Frameworks with Electronic Donor‐Acceptor System for Efficient Photocatalytic C−H Hydroxylation of Imidazole[1,2‐α]Pyridine Derivatives.
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- Chemistry - A European Journal, 2024, v. 30, n. 61, p. 1, doi. 10.1002/chem.202402246
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Cobalt Nanoparticles Catalyzed N‐Heterocycles Synthesis via Acceptorless Dehydrogenative Coupling.
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- Chemistry - A European Journal, 2024, v. 30, n. 56, p. 1, doi. 10.1002/chem.202402168
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Urea‐Promoted Neat Synthesis of Fused Dihydroisoquinolines and Disubstituted Pyridines: A Mechanistic Observation with Molecular‐Sensing Studies.
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- Chemistry - A European Journal, 2024, v. 30, n. 13, p. 1, doi. 10.1002/chem.202303287
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"Click" Chemistry for the Functionalization of Graphene Oxide with Phosphorus Dendrons: Synthesis, Characterization and Preliminary Biological Properties.
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- Chemistry - A European Journal, 2023, v. 29, n. 66, p. 1, doi. 10.1002/chem.202302198
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Visible Light and Triselenium Dicyanide (TSD): New Horizons in the Synthesis of Organic Selenocyanates.
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- Chemistry - A European Journal, 2023, v. 29, n. 59, p. 1, doi. 10.1002/chem.202301934
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Photoinduced Dehydrogenative Borylation via Dihydrogen Bond Bridged Electron Donor and Acceptor Complexes.
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- Chemistry - A European Journal, 2023, v. 29, n. 9, p. 1, doi. 10.1002/chem.202203053
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Anomeric Stereoauxiliary Cleavage of the C−N Bond of d‐Glucosamine for the Preparation of Imidazo[1,5‐a]pyridines.
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- Chemistry - A European Journal, 2022, v. 28, n. 29, p. 1, doi. 10.1002/chem.202200648
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Reactivity and Steric Parameters from 2D to 3D Bulky Pyridines: Increasing Steric Demand at Nitrogen with Chiral Azatriptycenes.
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- Angewandte Chemie, 2024, v. 136, n. 32, p. 1, doi. 10.1002/ange.202407503
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Accessing Pyridines via a Nitrene Internalization Process.
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- Angewandte Chemie, 2024, v. 136, n. 7, p. 1, doi. 10.1002/ange.202317228
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Electrocatalytic Synthesis of Pyridine Oximes using in Situ Generated NH<sub>2</sub>OH from NO species on Nanofiber Membranes Derived from NH<sub>2</sub>‐MIL‐53(Al).
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- Angewandte Chemie, 2023, v. 135, n. 45, p. 1, doi. 10.1002/ange.202312239
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Additive‐Free Transfer Hydrogenative Direct Asymmetric Reductive Amination Using a Chiral Pyridine‐Derived Half‐Sandwich Catalyst.
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- Angewandte Chemie, 2023, v. 135, n. 31, p. 1, doi. 10.1002/ange.202303709
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Catalytic Access to Chiral δ‐Lactams via Nucleophilic Dearomatization of Pyridine Derivatives.
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- Angewandte Chemie, 2023, v. 135, n. 9, p. 1, doi. 10.1002/ange.202217328
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Construction of Ultrastable Nonsubstituted Quinoline‐Bridged Covalent Organic Frameworks via Rhodium‐Catalyzed Dehydrogenative Annulation.
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- Angewandte Chemie, 2022, v. 134, n. 41, p. 1, doi. 10.1002/ange.202208833
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Alkyl/Glycosyl Sulfoxides as Radical Precursors and Their Use in the Synthesis of Pyridine Derivatives**.
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- Angewandte Chemie, 2022, v. 134, n. 31, p. 1, doi. 10.1002/ange.202204922
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Heteroatom‐Embedded Approach to Vinylene‐Linked Covalent Organic Frameworks with Isoelectronic Structures for Photoredox Catalysis.
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- Angewandte Chemie, 2022, v. 134, n. 6, p. 1, doi. 10.1002/ange.202111627
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Carbonyl Hypoiodites as Extremely Strong Halogen Bond Donors.
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- Angewandte Chemie, 2021, v. 133, n. 38, p. 20907, doi. 10.1002/ange.202108126
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Molecular Electrostatic Potential and Noncovalent Interactions in Derivatives of Group 8 Elements.
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- Angewandte Chemie, 2021, v. 133, n. 38, p. 20891, doi. 10.1002/ange.202107978
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Co‐assembled Supramolecular Gel of Dipeptide and Pyridine Derivatives with Controlled Chirality.
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- Angewandte Chemie, 2021, v. 133, n. 4, p. 2127, doi. 10.1002/ange.202012470
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Photorelease of Pyridines Using a Metal‐Free Photoremovable Protecting Group.
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- Angewandte Chemie, 2020, v. 132, n. 42, p. 18544, doi. 10.1002/ange.202005310
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Palladium‐Catalyzed Electrophilic Functionalization of Pyridine Derivatives through Phosphonium Salts.
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- Angewandte Chemie, 2020, v. 132, n. 38, p. 16556, doi. 10.1002/ange.202006724
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Synthesis and Neurotropic Activity of New Condensed Pyrano[4,3-b]-Pyridines Derivatives.
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- Pharmaceutical Chemistry Journal, 2019, v. 52, n. 10, p. 844, doi. 10.1007/s11094-019-1912-z
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Synthesis and Neurotropic Activity of 4-Phenylpyridine-3-Carboxylic Acid and 3-Hydroxy-4-Phenylthieno[2,3-b]-Pyridine Derivatives.
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- Pharmaceutical Chemistry Journal, 2019, v. 52, n. 10, p. 839, doi. 10.1007/s11094-019-1911-0
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Glucokinase Activators Based on N-Aryl-N′-Pyridin-2-Ylurea Derivatives.
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- Pharmaceutical Chemistry Journal, 2018, v. 52, n. 3, p. 209, doi. 10.1007/s11094-018-1792-7
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Synthesis and Fungi/Bactericidal Activities of 4-(4-Dimethylaminophenyl)Pyridine Derivatives.
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- Pharmaceutical Chemistry Journal, 2016, v. 50, n. 8, p. 526, doi. 10.1007/s11094-016-1482-2
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Synthesis and Neurotropic Activity of New Pyrano[3,4- b]Furo[2,3- b]Pyridine Derivatives.
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- Pharmaceutical Chemistry Journal, 2016, v. 49, n. 12, p. 830, doi. 10.1007/s11094-016-1381-6
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Synthesis and Neurotropic Activity of 8-Amino Derivatives of Condensed Thieno[3,2- d]- and Furo[3,2- d]Pyrimidines.
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- Pharmaceutical Chemistry Journal, 2014, v. 47, n. 12, p. 655, doi. 10.1007/s11094-014-1026-6
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Synthesis and neurotropic activity of new derivatives of piperazino-substituted pyrano[3,4- c]pyridines.
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- Pharmaceutical Chemistry Journal, 2013, v. 46, n. 10, p. 591, doi. 10.1007/s11094-013-0852-2
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Synthesis and antidepressant and anxiolytic activity of derivatives of pyrazolo[4,3- c]pyridine and 4-phenylhydrazinonicotinic acids.
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- Pharmaceutical Chemistry Journal, 2012, v. 46, n. 1, p. 15, doi. 10.1007/s11094-012-0726-z
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Chemical Structure of Pyridine Complexes Of Oxo(5,10,15,20-Tetraphenyl-21H,23H-Porphinato) Niobium(V) Chloride According to Formation Thermodynamics/Kinetics And Spectroscopy Data.
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- Journal of Structural Chemistry, 2018, v. 59, n. 8, p. 1880, doi. 10.1134/S0022476618080164
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Crystal structures of binuclear Bi(III) chloride and bromide complexes with some cations - Alkylated pyridine derivatives.
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- Journal of Structural Chemistry, 2017, v. 58, n. 4, p. 718, doi. 10.1134/S0022476617040114
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Single crystal X-ray diffraction study of 2,4,6-triazidopyridine and its 3,5-dibromosubstituted derivative.
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- Journal of Structural Chemistry, 2016, v. 57, n. 6, p. 1195, doi. 10.1134/S0022476616060202
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Theoretical view on structure, chemical reactivity, aromaticity and N NQR parameters of iridapyridine isomers.
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- Journal of Structural Chemistry, 2015, v. 56, n. 8, p. 1458, doi. 10.1134/S0022476615080028
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Theoretical study of solvent and substituent effects on the structure, N NQR and electronic spectra of [Cr(CO)py].
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- Journal of Structural Chemistry, 2015, v. 56, n. 8, p. 1474, doi. 10.1134/S0022476615080041
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Crystal structure and antitumor activities of the dichloride 2,6-bis(1-phenylbenzimidazol-2-yl)pyridine copper(II) complex.
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- Journal of Structural Chemistry, 2015, v. 56, n. 3, p. 458, doi. 10.1134/S0022476615030087
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Bioprocess development for nicotinic acid hydroxamate synthesis by acyltransferase activity of Bacillus smithii strain IITR6b2.
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- Journal of Industrial Microbiology & Biotechnology, 2013, v. 40, n. 9, p. 937, doi. 10.1007/s10295-013-1299-x
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Synthesis, cytotoxic assessment, and molecular docking studies of 2,6-diaryl-substituted pyridine and 3,4- dihydropyrimidine-2(1H)-one scaffolds.
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- Turkish Journal of Chemistry, 2020, v. 44, n. 1, p. 194, doi. 10.3906/kim-1903-72
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Synthesis and bioactivity of sulfide derivatives containing 1,3,4-oxadiazole and pyridine.
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- Turkish Journal of Chemistry, 2019, v. 43, n. 4, p. 1075, doi. 10.3906/kim-1901-45
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Tetrahydropyridine: a promising heterocycle for pharmacologically active molecules.
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- Turkish Journal of Chemistry, 2018, v. 42, n. 5, p. 1191, doi. 10.3906/kim-1709-4
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Synthesis and biological evaluation of new pyridines containing imidazole moiety as antimicrobial and anticancer agents.
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- Turkish Journal of Chemistry, 2015, v. 39, n. 2, p. 334, doi. 10.3906/kim-1410-25
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Thermal conversion of glycerol to value-added chemicals: pyridine derivatives by one-pot microwave-assisted synthesis.
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- Turkish Journal of Chemistry, 2014, v. 38, n. 4, p. 661, doi. 10.3906/kim-1312-47
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Electrochemical Grafting of a Pyridinium‐Conjugated Assembly on Graphite for H<sub>2</sub>O<sub>2</sub> Electrochemical Production.
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- ChemElectroChem, 2022, v. 9, n. 15, p. 1, doi. 10.1002/celc.202200395
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One-Pot Multi-Component Synthesis of Polysubstituted Pyridines Using DBU-SiO<sub>2</sub> as a Robust Recyclable Catalyst.
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- Polycyclic Aromatic Compounds, 2024, v. 44, n. 4, p. 2855, doi. 10.1080/10406638.2023.2225673
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Imparting aromaticity to 2-pyridone derivatives by O-alkylation resulted in new competitive and non-competitive PIM-1 kinase inhibitors with caspase-activated apoptosis.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2024, v. 39, n. 1, p. 1, doi. 10.1080/14756366.2024.2304044
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Design, synthesis and evaluation of 2, 6, 8-substituted Imidazopyridine derivatives as potent PI3Kα inhibitors.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2023, v. 38, n. 1, p. 1, doi. 10.1080/14756366.2022.2155638
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Biological evaluation, docking studies, and in silico ADME prediction of some pyrimidine and pyridine derivatives as potential EGFR<sup>WT</sup> and EGFR<sup>T790M</sup> inhibitors.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2023, v. 38, n. 1, p. 176, doi. 10.1080/14756366.2022.2135512
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Identification of 1H-pyrazolo[3,4-b]pyridine derivatives as novel and potent TBK1 inhibitors: design, synthesis, biological evaluation, and molecular docking study.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2022, v. 37, n. 1, p. 1411, doi. 10.1080/14756366.2022.2076674
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