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Recent Advances in the Synthesis of Fused‐Cyclic Quinolines.
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- Asian Journal of Organic Chemistry, 2024, v. 13, n. 5, p. 1, doi. 10.1002/ajoc.202400041
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- Article
Dibenzoindolo[1,8]naphthyridines: Synthesis and Characterization of X‐Shaped Aza[4,6]helicenes.
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- Chemistry - A European Journal, 2024, v. 30, n. 4, p. 1, doi. 10.1002/chem.202303225
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- Article
Antileishmanial Effect of 1,5- and 1,8-Substituted Fused Naphthyridines.
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- Molecules, 2024, v. 29, n. 1, p. 74, doi. 10.3390/molecules29010074
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- Article
Thermal Rearrangement of 5-(2-Hydroxy-6-oxocyclohexyl)-5 H -chromeno[2,3- b ]pyridines.
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- Molecules, 2023, v. 28, n. 7, p. 3139, doi. 10.3390/molecules28073139
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- Article
Preorganized Polyaromatic Soft Terdentate Hosts for the Capture of [Ln(β‐diketonate)<sub>3</sub>] Guests in Solution.
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- Chemistry - A European Journal, 2023, v. 29, n. 10, p. 1, doi. 10.1002/chem.202202727
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- Article
Synthesis of Novel Benzo[ b ][1,6]naphthyridine Derivatives and Investigation of Their Potential as Scaffolds of MAO Inhibitors.
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- Molecules, 2023, v. 28, n. 4, p. 1662, doi. 10.3390/molecules28041662
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- Article
Environmentally favorable Synthesis and Characterization of series of 2-hydrazinyl-3- substituted [1,8] naphthyridines.
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- Journal of Pharmaceutical Negative Results, 2023, v. 14, p. 1921, doi. 10.47750/pnr.2023.14.S02.230
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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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Oxidative Cyclization of 5 H -Chromeno[2,3- b ]pyridines to Benzo[ b ]chromeno[4,3,2- de ][1,6]naphthyridines, Their NMR Study and Computer Evaluation as Material for LED.
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- Molecules, 2022, v. 27, n. 13, p. 4156, doi. 10.3390/molecules27134156
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- Article
Iodine‐Catalyzed Annulations of 2‐Amino Carbonyls for Diverse 1‐Azaxanthones, Quinolines, and Naphthyridines.
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- Asian Journal of Organic Chemistry, 2021, v. 10, n. 10, p. 2670, doi. 10.1002/ajoc.202100568
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- Article
1,6-Naphthyridin-2(1 H)-ones: Synthesis and Biomedical Applications.
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- Pharmaceuticals (14248247), 2021, v. 14, n. 10, p. 1029, doi. 10.3390/ph14101029
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- Article
Biological Activity of Naturally Derived Naphthyridines.
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- Molecules, 2021, v. 26, n. 14, p. 4324, doi. 10.3390/molecules26144324
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ZnO/Ag/Fe<sub>3</sub>O<sub>4</sub> nanoparticles supported on carbon nanotubes employing Petasites hybridus rhizome water extract: A novel organometallic nanocatalyst for the synthesis of new naphthyridines.
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- Applied Organometallic Chemistry, 2021, v. 35, n. 3, p. 1, doi. 10.1002/aoc.6114
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Synthesis of Novel Tetrahydropyrimido[4,5-B][1,6]Naphthyridines via Condensation of 1-benzyl-3,5-bis[(E)-arylmethylidene]tetrahydropyridin-4(1H)-ones with 6-aminouracils.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 11, p. 1473, doi. 10.1007/s10593-020-02840-z
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Thermolysis of 3-azido-4-aryl(hetaryl)thieno[2,3-b]pyridines: 2,7-naphthyridines or 1,4-diazepines?
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- Chemistry of Heterocyclic Compounds, 2019, v. 55, n. 9, p. 882, doi. 10.1007/s10593-019-02552-z
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- Article
Design, synthesis, and biological evaluation of 1,8‐naphthyridine glucosamine conjugates as antimicrobial agents.
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- Drug Development Research, 2019, v. 80, n. 1, p. 179, doi. 10.1002/ddr.21508
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- Article
A Novel Naphthyridine Derivative, 3u, Induces Necroptosis at Low Concentrations and Apoptosis at High Concentrations in Human Melanoma A375 Cells.
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- International Journal of Molecular Sciences, 2018, v. 19, n. 10, p. 2975, doi. 10.3390/ijms19102975
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- Article
Fluorescent Trimethylated Naphthyridine Derivative with an Aminoalkyl Side Chain as the Tightest Non‐aminoglycoside Ligand for the Bacterial A‐site RNA.
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- Chemistry - A European Journal, 2018, v. 24, n. 52, p. 13862, doi. 10.1002/chem.201802320
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The First 1-Hydroxypropylidenebisphosphonic Acid with 1,8-Naphthyridinone Substituent: Synthesis and Structure.
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- Russian Journal of General Chemistry, 2018, v. 88, n. 9, p. 1792, doi. 10.1134/S1070363218090050
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Fluorescent Zn<sup>II</sup> Chemosensor Mediated by a 1,8‐Naphthyridine Derivative and It′s Photophysical Properties.
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- ChemistryOpen, 2018, v. 7, n. 8, p. 639, doi. 10.1002/open.201800083
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Synthesis of New 5-Aryl-benzo[f][1,7]naphthyridines via a Cascade Process (Ugi-3CR/Intramolecular Aza-Diels-Alder Cycloaddition)/Aromatization.
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- Molecules, 2018, v. 23, n. 8, p. 2029, doi. 10.3390/molecules23082029
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Merging Visible‐Light Photoredox and Lewis Acid Catalysis for the Intramolecular Aza‐Diels–Alder Reaction: Synthesis of Substituted Chromeno[4,3‐b]quinolines and [1,6]Naphthyridines.
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- ChemCatChem, 2018, v. 10, n. 13, p. 2878, doi. 10.1002/cctc.201800192
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Cascade methods for the synthesis of annulated 1,8-naphthyridines (microreview).
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- Chemistry of Heterocyclic Compounds, 2018, v. 54, n. 7, p. 689, doi. 10.1007/s10593-018-2332-9
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- Article
Green Synthesis and Biological Evaluation of Novel Fused 6-(2-Chloro-4-fluorophenyl)-9-arylimidazo[1,2-a][1,8]naphthyridine Derivatives Catalyzed by DABCO.
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- Russian Journal of General Chemistry, 2018, v. 88, n. 7, p. 1495, doi. 10.1134/S107036321807023X
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- Article
Ferric Chloride-catalyzed Synthesis of 2-Oxo-1,2-dihydro-1,8-naphthyridine-3-carboxylate Derivatives and Their Biological Evaluation.
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- Russian Journal of General Chemistry, 2018, v. 88, n. 6, p. 1224, doi. 10.1134/S1070363218060294
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- Article
A 1,5‐Naphthyridine‐Fused Porphyrin Dimer: Intense NIR Absorption and Facile Redox Interconversion with Its Reduced Congener.
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- Chemistry - A European Journal, 2018, v. 24, n. 25, p. 6530, doi. 10.1002/chem.201800854
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- Article
Synthesis and Neurotropic Activity of New 7-Cyclohexyl-6,7,8,9-Tetrahydro-3H-Pyrazolo[3,4-c]-2,7-Naphthyridine-1,5-Diamines.
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- Pharmaceutical Chemistry Journal, 2018, v. 52, n. 2, p. 108, doi. 10.1007/s11094-018-1773-x
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- Article
Efficient three-component synthesis of 5-(6-hydroxy-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)-5,12-dihydrobenzo[<italic>b</italic>]pyrimido[5,4-<italic>g</italic>][1,8]naphthyridine-2,4(1<italic>H</italic>,3<italic>H</italic>)-dione.
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- Heterocyclic Communications, 2018, v. 24, n. 2, p. 75, doi. 10.1515/hc-2017-0265
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Safety Evaluation of repeated oral administration of Gemifloxacin in Broiler Birds.
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- Indian Journal of Veterinary Sciences & Biotechnology, 2018, v. 13, n. 4, p. 1, doi. 10.21887/ijvsbt.v13i4.11549
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- Article
An Efficient Microwave-Assisted Synthesis of Novel 2-{4-[(3-Aryl-1,8-naphthyridin-2-yl)amino]phenyl}-1H-benzo[de]isoquinoline-1,3(2H)-diones and Their Antimicrobial Activity.
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- Russian Journal of General Chemistry, 2018, v. 88, n. 4, p. 780, doi. 10.1134/S1070363218040242
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- Article
How to Translate the [LCu<sub>2</sub>(H)]<sup>+</sup>‐Catalysed Selective Decomposition of Formic Acid into H<sub>2</sub> and CO<sub>2</sub> from the Gas Phase into a Zeolite.
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- ChemCatChem, 2018, v. 10, n. 5, p. 1173, doi. 10.1002/cctc.201701594
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The crystal structure of a matrine derivative: 4<sup>1</sup><italic>S</italic>,7a<italic>S</italic>,12<italic>S</italic>,13a<italic>R</italic>,13b<italic>R</italic>)-12-(4-methylpiperazin-1-yl)dodecahydro-1<italic>H</italic>,5<italic>H</italic>,10<italic>H</italic>-dipyrido[2,1-<italic>f</italic>:3′,2′,1′-<italic>ij</italic>][1,6]naphthyridin-10-one, C<sub>20</sub>H<sub>34</sub>N<sub>4</sub>O
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- Zeitschrift für Kristallographie / New Crystal Structures, 2018, v. 233, n. 2, p. 283, doi. 10.1515/ncrs-2017-0282
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Designing 1,5‐Naphthyridine‐2,6‐dione‐Based Conjugated Polymers for Higher Crystallinity and Enhanced Light Absorption to Achieve 9.63% Efficiency Polymer Solar Cells.
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- Advanced Energy Materials, 2018, v. 8, n. 2, p. 1, doi. 10.1002/aenm.201701467
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- Article
ENVIRONMENTALLY BENIGN SYNTHESIS AND ANTIBACTERIAL ACTIVITY OF 1-[3-(2-NAPHTHYL)[1,8]NAPHTHYRIDIN-2-YL]-3-(2-OXO-2H-3-CHROMENYL)-1H-4-PYRAZOLECARBALDEHYDES.
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- International Journal of Pharmaceutical, Chemical & Biological Sciences, 2018, v. 8, n. 1, p. 134
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Synthesis of Naphthyridine Dimers with Conformational Restriction and Binding to DNA and RNA.
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- Chemistry - An Asian Journal, 2017, v. 12, n. 23, p. 3077, doi. 10.1002/asia.201701293
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- Article
Synthesis and Biological Evaluation of Some Novel 1,8-Naphthyridine Derivatives.
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- Acta Chimica Slovenica, 2017, v. 64, n. 4, p. 919, doi. 10.17344/acsi.2017.3617
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- Article
Multi Component Reactions under Increased Pressure: On the Mechanism of Formation of Pyridazino[5,4,3-de][1,6]naphthyridine Derivatives by the Reaction of Malononitrile, Aldehydes and 2-Oxoglyoxalarylhydrazones in Q-Tubes.
- Published in:
- Molecules, 2017, v. 22, n. 12, p. 2114, doi. 10.3390/molecules22122114
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Hydrogen-Transfer-Mediated α-Functionalization of 1,8-Naphthyridines by a Strategy Overcoming the Over-Hydrogenation Barrier.
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- Angewandte Chemie, 2017, v. 129, n. 45, p. 14420, doi. 10.1002/ange.201707702
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- Article
The crystal structure of the Matrine derivative: 12-(1H-indol-1-yl) dodecahydro-1H,5H,10H-dipyrido[2,1-f :3',2',1'-ij][1,6]naphthyridin-10-one hydrate, C<sub>23</sub>H<sub>29</sub>N<sub>3</sub>O.
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- Zeitschrift für Kristallographie / New Crystal Structures, 2017, v. 232, n. 6, p. 1017, doi. 10.1515/ncrs-2017-0144
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- Article
MICROWAVE ASSISTED SYNTHESIS OF 4-AZETIDINONE DERIVATIVES OF 1, 8-NAPHTHYRIDINE.
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- Rasayan Journal of Chemistry, 2017, v. 10, n. 4, p. 1094, doi. 10.7324/RJC.2017.1041868
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- Article
SYNTHESIS AND ANTIBACTERIAL ACTIVITY OF 2-((3/4-(1,8- NAPHTHYRIDIN-2-YL)PHENOXY)METHYL)-NPHENYLBENZAMIDE DERIVATIVES.
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- Rasayan Journal of Chemistry, 2017, v. 10, n. 4, p. 1521, doi. 10.7324/RJC.2017.1041920
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Synthesis and reactions of some novel 1-(2,7-dimethyl-1,8-naphthyridin-4-yl)hydrazine candidates.
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- Russian Journal of General Chemistry, 2017, v. 87, n. 10, p. 2462, doi. 10.1134/S1070363217100292
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- Article
Synthesis of new tetrahydrobenzo[ b]pyrimido- [5,4- g][1,8]naphthyridine-2,4-diones from 6-aminouracils.
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- Russian Journal of Organic Chemistry, 2017, v. 53, n. 10, p. 1609, doi. 10.1134/S1070428017100232
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- Article
(OC-6-35-A)-Aquadicarbonylchlorido[2-(2-pyridyl)-1,8-Naphthyridine-κ<sup>2</sup>N<sup>1</sup>,N<sup>2</sup>]Ruthenium(II) Hexafluoridophosphate 2,2'-Bipyridine.
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- Molbank, 2017, v. 2017, n. 3, p. m950, doi. 10.3390/M950
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- Article
Hydrogen-transfer reduction of α,β-unsaturated carbonyl compounds catalyzed by naphthyridine-functionalized N-heterocyclic carbene complexes.
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- Applied Organometallic Chemistry, 2017, v. 31, n. 8, p. n/a, doi. 10.1002/aoc.3673
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- Article
One-pot synthesis of annulated 1,8-naphthyridines.
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- Heterocyclic Communications, 2017, v. 23, n. 4, p. 269, doi. 10.1515/hc-2017-0068
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- Article
A novel and efficient synthesis of 3-iodo substituted 1,8-naphthyridines by electrophilic cyclization of 2-amino nicotinaldehyde and their antimicrobial activity.
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- Russian Journal of General Chemistry, 2017, v. 87, n. 8, p. 1794, doi. 10.1134/S1070363217080266
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Synthesis of fused derivatives of 1,8-naphthyridine.
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- Russian Journal of Organic Chemistry, 2017, v. 53, n. 8, p. 1243, doi. 10.1134/S1070428017080140
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- Article
Antilipolytic effects of 1,8-naphthyridine derivatives β-adrenoceptor antagonists in rat white adipocytes.
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- Chemical Biology & Drug Design, 2017, v. 90, n. 1, p. 119, doi. 10.1111/cbdd.12933
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Synthesis and antitumor activity against HepG-2, PC-3, and HCT-116 cells of some naphthyridine and pyranopyridinecarbonitrile derivatives.
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- Russian Journal of General Chemistry, 2017, v. 87, n. 6, p. 1264, doi. 10.1134/S1070363217060226
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- Article