Relevant bibliographies by topics / Methyl quinoline

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers
  5. Reports

Academic literature on the topic 'Methyl quinoline'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Methyl quinoline"

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Horta, Pedro, Marta S. C. Henriques, Elisa M. Brás, et al. "On the ordeal of quinolone preparation via cyclisation of aryl-enamines; synthesis and structure of ethyl 6-methyl-7-iodo-4-(3-iodo-4-methylphenoxy)-quinoline-3-carboxylate." Pure and Applied Chemistry 89, no. 6 (2017): 765–80. http://dx.doi.org/10.1515/pac-2016-1119.

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AbstractRecent studies directed to the design of compounds targeting the bc1 protein complex of Plasmodium falciparum, the parasite responsible for most lethal cases of malaria, identified quinolones (4-oxo-quinolines) with low nanomolar inhibitory activity against both the enzyme and infected erythrocytes. The 4-oxo-quinoline 3-ester chemotype emerged as a possible source of potent bc1 inhibitors, prompting us to expand the library of available analogs for SAR studies and subsequent lead optimization. We now report the synthesis and structural characterization of unexpected ethyl 6-methyl-7-i
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Portilla, Jaime, Jairo Quiroga, Manuel Nogueras, et al. "Structural comparisons of isomeric series of 7-aryl-benzo[h]pyrazolo[3,4-b]quinolines and 11-aryl-benzo[f]pyrazolo[3,4-b]quinolines." Acta Crystallographica Section B Structural Science 64, no. 1 (2008): 72–83. http://dx.doi.org/10.1107/s0108768107065743.

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The structures of three new 7-aryl-benzo[h]pyrazolo[3,4-b]quinolines, 8-methyl-7-(4-chlorophenyl)-10-phenyl-6,10-dihydro-5H-benzo[h]pyrazolo[3,4-b]quinoline, C27H20ClN3, 8-methyl-7-(3-pyridinyl)-10-phenyl-6,10-dihydro-5H-benzo[b]pyrazolo[3,4-b]quinoline, C26H20N4, and 8-methyl-7-(4-pyridinyl)-10-phenyl-10H-benzo[h]pyrazolo[3,4-b]quinoline, C26H18N4, which is an unexpected oxidation product isolated from the attempted synthesis of 8-methyl-7-(4-pyridinyl)-10-phenyl-6,10-dihydro-5H-benzo[h]pyrazolo[3,4-b]quinoline, and those of three new 11-aryl-benzo[f]pyrazolo[3,4-b]quinolines, 11-(4-methylphe
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Schmidt, Alexander, Matthias Baune, Alexander Hepp, Jutta Kösters, and Jens Müller. "Gold(III)-mediated cyclization of 2-hydrazinylquinolines." Zeitschrift für Naturforschung B 71, no. 5 (2016): 527–33. http://dx.doi.org/10.1515/znb-2016-0021.

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AbstractThe Au(III)-mediated oxidative cyclization of a series of 2-hydrazinylquinolines is reported. This intramolecular reaction represents a reliable way towards obtaining various 3H-1,2,4-triazolo[4,3-a]quinolin-10-ium cations. The molecular structures of three of the starting compounds (2-(1-methyl-2-(pyridin-2-ylmethylene)hydrazinyl)quinoline, 2-(1-methyl-2-(thiophen-2-ylmethylene)hydrazinyl)quinoline, 2-((2-methyl-2-(quinolin-2-yl)hydrazono)methyl)aniline) as well as of one cyclized system (3-methyl-1-(pyridin-2-yl)-3H-1,2,4-triazolo[4,3-a]quinolin-10-ium dichloridoaurate(I)) were deter
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Elagamey, Abdel Ghani A., Salah Z. Sawllim, Fathy M. A. El-Taweel, and Mohamed H. Elnagdi. "Nitriles in heterocyclic synthesis: Novel syntheses of benzo[b]pyrans, naphtho[1,2-b]pyrans, naphtho[2,1-b]pyrans, pyrano[3,2-h]quinolines and pyrano[3,2-c]quinolines." Collection of Czechoslovak Chemical Communications 53, no. 7 (1988): 1534–38. http://dx.doi.org/10.1135/cccc19881534.

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Benzo[b]pyrans, naphtho[1,2-b]pyrans, naphtho[2,1-b]pyrans, pyrano[3,2-h]quinolines, and pyrano[3,2-c]quinolines were synthesized by the reaction of cinnamonitriles with phenols, naphthols, 8-hydroxyquinoline, and 1-methyl-4-hydroxy-2-quinoline.
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Faldu, V. J., P. K. Talpara, N. H. Bhuva, P. R. Vachharajani, and Viresh H. Shah. "Synthesis, Characterization and Biological Evaluation of some Newer 5-[6-Chloro/Fluor/Nitro-2-(p-Chloro/Fluoro/Methyl Phenyl)-Quinolin-4-yl]-1,3,4-Oxadiazole-2-Thiols." International Letters of Chemistry, Physics and Astronomy 25 (January 2014): 26–32. http://dx.doi.org/10.18052/www.scipress.com/ilcpa.25.26.

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Recent study shows that quinolines represent one of the most active classes of compounds possesses wide spectrum biodynamic activities and use as potent therapeutic agents. In present research work, 5-[6-chloro/fluoro/nitro-2-(p-chloro/fluoro/methyl phenyl)-quinolin-4-yl]-1,3,4-oxadiazole-2-thiols have been synthesized by condensation of substituted quinoline-4-carbohydrazides and mixture of carbon disulphide and potassium hydroxide. All of these compounds were screened for their in vitro anti microbial assay against gram (+ve), gram (-ve) bacteria and fungi activity compared with standard dru
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Faldu, V. J., P. K. Talpara, N. H. Bhuva, P. R. Vachharajani, and Viresh H. Shah. "Synthesis, Characterization and Biological Evaluation of some Newer 5-[6-Chloro/Fluor/Nitro-2-(p-Chloro/Fluoro/Methyl Phenyl)-Quinolin-4-yl]-1,3,4-Oxadiazole-2-Thiols." International Letters of Chemistry, Physics and Astronomy 25 (January 10, 2014): 26–32. http://dx.doi.org/10.56431/p-vi5cvh.

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Recent study shows that quinolines represent one of the most active classes of compounds possesses wide spectrum biodynamic activities and use as potent therapeutic agents. In present research work, 5-[6-chloro/fluoro/nitro-2-(p-chloro/fluoro/methyl phenyl)-quinolin-4-yl]-1,3,4-oxadiazole-2-thiols have been synthesized by condensation of substituted quinoline-4-carbohydrazides and mixture of carbon disulphide and potassium hydroxide. All of these compounds were screened for their in vitro anti microbial assay against gram (+ve), gram (-ve) bacteria and fungi activity compared with standard dru
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Kamal, Ahmed, Abdul Rahim, Sd Riyaz, et al. "Regioselective synthesis, antimicrobial evaluation and theoretical studies of 2-styryl quinolines." Organic & Biomolecular Chemistry 13, no. 5 (2015): 1347–57. http://dx.doi.org/10.1039/c4ob02277g.

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2-Styryl quinolines have been synthesized regioselectively from 2-methyl-quinoline using NaOAc in water acetic acid binary solvents and evaluated for their antibacterial activity against both Gram-positive and Gram-negative strains.
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Radini, Ibrahim Ali, Sameh Ramadan El-Gogary, Mohamed Sabri Mostafa, Bander Alnagei, Mohammed Mudarbish, and Shadad Dash. "Ecofriendly and simple synthesis of pyrano[3,2-c]quinolone in water via an efficient one-pot three-component reaction." European Journal of Chemistry 9, no. 1 (2018): 44–48. http://dx.doi.org/10.5155/eurjchem.9.1.44-48.1679.

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Pyrano[3,2-c]quinolones are commonly found in alkaloids, manifesting diverse biological activities. In this work, 2-amino-6-methyl-5-oxo-4-substituted-5,6-dihydro-4H-pyrano[3,2-c]quinoline-3-carbonitriles and ethyl 2-amino-4-(substituted)-6-methyl-5-oxo-5,6-dihydro-4H-pyrano[3,2-c]quinoline-3-carboxylates have been synthesized efficiently from reaction of 4-hydroxy-1-methylquinolin-2(1H)-one, aldehydes and active methylene nitriles in one-pot three component reaction in aqueous medium, containing catalytic amount of ethanolamine resulting in 70-95% yields.
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Provatas, Anthony A., Gary A. Epling, and James D. Stuart. "Synthesis and Photocleavage of Quinoline Methyl Ethers: A Mild and Efficient Method for the Selective Protection and Deprotection of the Alcohol Functionality." Australian Journal of Chemistry 69, no. 7 (2016): 763. http://dx.doi.org/10.1071/ch15627.

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The synthesis and photocleavage of quinolinyl methyl ether-protected alcohols is reported in this study. A variety of quinoline methyl chlorides were synthesized, and protection of the various alcohols was performed via a substitution reaction in the presence of a strong base. Photocleavage of the quinolinyl methyl ether moiety proceeded under visible light with the formation of the charged quinolinyl radical intermediate through a single-electron transfer in the presence of a photosensitizer dye leading to the deprotected alcohol in excellent yields. The utility of triethylamine as a sacrific
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Munir, Rubina, Noman Javid, Muhammad Zia-ur-Rehman, et al. "Synthesis of Novel N-Acylhydrazones and Their C-N/N-N Bond Conformational Characterization by NMR Spectroscopy." Molecules 26, no. 16 (2021): 4908. http://dx.doi.org/10.3390/molecules26164908.

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In this article, a synthesis of N’-(benzylidene)-2-(6-methyl-1H-pyrazolo[3,4-b]quinolin-1-yl)acetohydrazides and their structural interpretation by NMR experiments is described in an attempt to explain the duplication of some peaks in their 1H- and 13C-NMR spectra. Twenty new 6-methyl-1H-pyrazolo[3,4-b]quinoline substituted N-acylhydrazones 6(a–t) were synthesized from 2-chloro-6-methylquinoline-3-carbaldehyde (1) in four steps. 2-Chloro-6-methylquinoline-3-carbaldehyde (1) afforded 6-methyl-1H-pyrazolo[3,4-b]quinoline (2), which upon N-alkylation yielded 2-(6-methyl-1H-pyrazolo[3,4-b]quinolin
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Dissertations / Theses on the topic "Methyl quinoline"

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Horn, Mark A. "Studies toward the synthesis of the A-B ring system of lavendamycin methyl ester." Virtual Press, 1987. http://liblink.bsu.edu/uhtbin/catkey/515490.

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The synthesis of 7-amino-2-methylquinoline-5-8-dione (17) and 7-amino-3-methylquinoline-5,8-dione (157) are described.7-Amino-3-methylquinoline-5,8-dione (157) was prepared via alkaline hydrolysis of 7-acetamido-3-methylquinoline5,8-dione (149). 7-Acetamido-3-methylquinoline-5,8-dione (149) was prepared via the Diels-Alder reaction of 2-acetamido-6-bromo-1,4-benzoquinone (6) and 2-methyl-2propenal dimethylhydrazone (110).7-Amino-2-methylquinoline-5,8-dione (17) was prepared by the acid hydrolysis of 7-(triphenylphosphineimino)-2methylquinoline-5,8-dione (16). 7-(Triphenylphosphineimino)2-methy
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Morgan, Elaine M. "The role of nitric oxide in N-methyl-D-aspartate receptor-mediated neurotoxicity." Thesis, University of Southampton, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.243084.

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Deraeve, Céline. "Synthèse et évaluation biologique de dérivés polyquinoléine chélateurs d'ions métalliques en relation avec la maladie d'Alzheimer." Phd thesis, Université Paul Sabatier - Toulouse III, 2006. http://tel.archives-ouvertes.fr/tel-00142741.

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Les ions métalliques ZnII, CuII et FeIII interagissent avec le peptide b-amyloïde (Ab) dans la maladie d'Alzheimer. Ils participent à la précipitation d'A_ et à sa toxicité via la production d'H2O2. Une stratégie thérapeutique consiste à chélater ces ions métalliques par des ligands hétérocycliques reliés de façon covalente afin d'augmenter leur affinité pour ces ions. Parmi eux, la Cyclo-bi-Phen diminue les plaques amyloïdes de souris transgéniques modélisant la maladie d'Alzheimer. Une nouvelle série a été établie à partir du clioquinol, un ligand quinoléine actif in vitro et in vivo. Plus d
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Sommer, Samantha. "Hybrid Metal-Ligand Hydrogen-Bonded (MLHB) Architectures Based on the Quinolone Subunit: Understanding and Expanding the Accessible Space of Supramolecular Systems." Thesis, University of Oregon, 2015. http://hdl.handle.net/1794/19298.

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Despite the prevalence of supramolecular architectures derived from metal-ligand or hydrogen-bonding interactions, few studies have focused on the simultaneous use of these two strategies to form discrete metal-ligand hydrogen-bonded (MLHB) assemblies. The design, synthesis, and characterization of 2-quinolone based hybrid subunits, 7-DPQ and 5-PYQ, that contain phosphine and pyridyl metal binding sites, respectively, is reported. Both subunits give two-fold symmetric hydrogen-bonded tectons that assemble with metal precursors to give hybrid MLHB structures. Treatment of [Cp*RhCl2]2 with t
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Coulibaly, Gnougon Nina. "Élimination des antibiotiques quinolones sur des catalyseurs supportés : Applications sur des effluents hospitaliers." Thesis, Rennes, Ecole nationale supérieure de chimie, 2019. https://www.ensc-rennes.fr/formations/doctorats.

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L'usage excessif des antibiotiques en médecine humaine et animale pose de graves problèmes environnementaux et de santé publique. L’objectif de cette thèse était d’éliminer deux types d’antibiotiques quinolones pouvant être détectés dans des eaux usées ou effluents hospitaliers. Dans un premier temps, nous avons évalué la réactivité d’oxydes métalliques (fer ou zinc) pour promouvoir des réactions d’oxydation avancée, en présence d’oxydants comme le peroxyde d’hydrogène, le persulfate ou le peroxymonosulfate, et sous irradiation (UVA ou visible). Les oxydes réactifs étaient supportés sur des me
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Fournel, Jean-Louis. "Synthèse et étude de nouveaux agonistes dopaminergiques : les amino hydroxy tetrahydro quinoléines." Rouen, 1986. http://www.theses.fr/1986ROUES029.

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Synthèse d'hydroxy- ou dihydroxy amino-3 tetrahydro-1,2,3,4 quinoléines par réduction par NABH4 ou par hydrogénations sur palladium d'amino-3 quinoléines ; études de relation structure activité ; calculs MNDO et CNDO
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Chi, Li-Jen. "Synthesis and computer-aided structural investigation of potentially photochromic spirooxazines." Thesis, Heriot-Watt University, 2000. http://hdl.handle.net/10399/564.

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Bipath, Priyesh. "Tryptophan and the kynurenine pathway in chronic renal failure patients on dialysis." Diss., Pretoria : [s.n.], 2008. http://upetd.up.ac.za/thesis/available/etd-10212008-135418.

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Boukhalfa, Hakim. "Complexation du fer par des ligands tripodes à base de sous-unités 8-hydroxyquinoléine et 2,2'dihydroxybiphényle : aspects thermodynamiques et cinétiques." Université Joseph Fourier (Grenoble), 1996. http://www.theses.fr/1996GRE10250.

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Ce travail concerne des etudes thermodynamiques et cinetiques de la complexation du fer(iii) par des ligands possedant des sites de coordination de type 8-hydroxyquinoleine et 2,2'-dihydroxybiphenyle. La premiere partie a concerne l'etude des complexes ferriques des ligands 8-hq (oxine), 5-so#3#, 8-hq (sulfoxine) et 5-f-8-hq (fluorooxine). Les resultats mettent en evidence l'influence des proprietes electroniques des sites de coordination sur la stabilite des complexes. Quand la coordination du fer par le ligand n'est pas complete, des hydroxo complexes sont formes. Les etudes cinetiques de fo
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Demonchaux, Patrice. "Recherche d'agents radioprotecteurs : synthèse et mécanisme d'action de composés de type intercalant-aminothiol." Grenoble 1, 1988. http://www.theses.fr/1988GRE10016.

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Les intercalants utilises sont des amino-9 chloro-6 methoxy-2 acridines des amino-4 chloro-7 quinoleines et des amino-4 chloro-7 methyl-1 quinoleiniums sur lesquels ont ete introduites des chaines analogues a celles de la cysteamine et du wr 2727; etude de l'affinite de ces composes avec l'adn
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Book chapters on the topic "Methyl quinoline"

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Winkelmann, J. "Diffusion of oxygen (1); 2-methyl-quinoline (2)." In Gases in Gases, Liquids and their Mixtures. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-49718-9_296.

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Winkelmann, J. "Diffusion of oxygen (1); 3-methyl-quinoline (2)." In Gases in Gases, Liquids and their Mixtures. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-49718-9_297.

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Winkelmann, J. "Diffusion of oxygen (1); 4-methyl-quinoline (2)." In Gases in Gases, Liquids and their Mixtures. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-49718-9_298.

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Winkelmann, J. "Diffusion of oxygen (1); 6-methyl-quinoline (2)." In Gases in Gases, Liquids and their Mixtures. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-49718-9_299.

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Winkelmann, J. "Diffusion of oxygen (1); 7-methyl-quinoline (2)." In Gases in Gases, Liquids and their Mixtures. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-49718-9_300.

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Winkelmann, J. "Diffusion of oxygen (1); 8-methyl-quinoline (2)." In Gases in Gases, Liquids and their Mixtures. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-49718-9_301.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of nickel(II) 3-methylbenzoate adduct with 4-methyl quinoline." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54234-7_22.

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Yokoshima, Satoshi. "Construction of Quinoline N-Oxides and Synthesis of Aurachins A and B: Discovery, Application, and Mechanistic Insight." In Modern Natural Product Synthesis. Springer Nature Singapore, 2024. http://dx.doi.org/10.1007/978-981-97-1619-7_17.

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AbstractA method to synthesize 3-hydroxyquinoline N-oxides from ketones having a 2-nitrophenyl group at the α-position relative to the carbonyl group was developed. The substrates were easily prepared via a SNAr reaction or a Sonogashira coupling, and treatment with sodium tert-butoxide in dimethyl sulfoxide produced the corresponding quinoline N-oxides. The method was successfully applied to the total synthesis of aurachins A and B. On the basis of the quinoline N-oxide synthesis, related reactions of α-(2-nitrophenyl)ketones, including nitrone formation and photoinduced rearrangement, were a
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Ruan, J. Z., and M. H. Litt. "Synthesis and Electronic Properties of Poly(8-methyl-2,3-6,7-quinolino) and Its Intermediate." In Polymers for High Technology. American Chemical Society, 1987. http://dx.doi.org/10.1021/bk-1987-0346.ch048.

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Amati, Mario, and Francesco Lelj. "Electronic Properties, Spectroscopic Properties and Monomolecular Isomerization Processes of Prototype OLED Compound Aluminum Tris(Quinolin-8-Olate) Facial and Meridianal Isomers." In Metal-Ligand Interactions. Springer Netherlands, 2003. http://dx.doi.org/10.1007/978-94-010-0191-5_14.

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Conference papers on the topic "Methyl quinoline"

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Lukovits, I., T. Kosztolányi, E. Kálmán, and G. Pálinkás. "Corrosion Inhibitors: Correlation between Chemical Structure and Efficiency." In CORROSION 1999. NACE International, 1999. https://doi.org/10.5006/c1999-99242.

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Abstract Corrosion inhibition efficiencies of heterocyclic, aromatic or partially saturated aromatic compounds (pyrimidines, benzothiazole derivatives, amino-acids containing an aromatic part, pyridines and quinolines) were correlated with quantum chemical indices of the respective molecules. Inhibition efficiencies measured in acidic solutions containing 0.001 and 0.01 mol/L of the inhibitor, respectively, were collected. The quantum chemical calculations were done by using the simple Hückel method. Comparison of inhibition efficiencies and the differences between energies of the highest occu
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Christie, D. J., H. Diaz-Arauzo, and J. M. Cook. "REACTIONS OF DRUG-DEPENDENT ANTIBODIES WITH METABOLITES OF QUININE (Qn) AND QUINIDINE (Qd)." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644578.

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In many cases of drug-induced immunologic thrombocytopenia (DITP), a metabolite, rather than the native drug, is suspected of provoking the destructive drug-dependent antibodies (DDAB) responsible for this severe hemorrhagic disorder. However, this has not previously been investigated for Qn- and Qd-DDAB. We report evidence that the native drugs, and not their metabolites, are the provocative agents in Qn and Qd DITP. Reactions of Qn- and Qd-DDAB with platelets were studied with the native drugs and four of their metabolites: the N-oxide and 10,11-diol derivatives (quinuclidine ring modificati
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Kumar, Rahul, and Parag Bhargava. "Synthesis and characterization of a new photoluminescent material tris (2-methyl-8-hydroxy quinoline) lanthanum La(mq)3." In DAE SOLID STATE PHYSICS SYMPOSIUM 2015. Author(s), 2016. http://dx.doi.org/10.1063/1.4948172.

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Rasheed, Anaam M., Sinan M. Al-bayati, and Mahmoud Najim Al-jibouri. "Synthesis, spectroscopic and thermal studies of some transition metals complexes derived from 1-hydrazino-7-octyloxy-4-methyl-quinoline." In INTERNATIONAL CONFERENCE OF NUMERICAL ANALYSIS AND APPLIED MATHEMATICS ICNAAM 2019. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0030058.

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Manabe, S., H. Yanagisawa, S. Ishikawa, et al. "TRYPTOPHAN PYROLYSIS PRODUCTS FOUND IN COOKED FOODS INHIBIT HUMAN PLATELET AGGREGATION BY INHIBITING CYCLOOXYGENASE." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643402.

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Humans are exposed to numerous toxic compounds in foods. During the past decade, several carcinogenic heterocyclic amines have been reported to be present in the cooked foods. Recently, we reported that some of the carcinogenic heterocyclic amines isolated from foods were present in human plasma. In order to know the effects of the carcinogens isolated from foods on the cell function, we investigated the effects of the carcinogenic heterocyclic amines including Trp-P-1(3-amino-l,4-dimethyl-5H-pyrido❘4,3-b❘indole) and Trp-P-2(3-amino-1-methyl-5H-pyrido❘4,3-b❘indole) on human platelet aggregatio
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DIACONU, Dumitrela, Violeta MANGALAGIU, Roxana CIORTEANU, and Ionel I. MANGALAGIU. "MATERIALS BASED ON QUINOLINE SULFONAMIDE - METALS WITH ANTIMICROBIAL ACTIVITY AND THEIR X-Ray characterisation." In METAL 2022. TANGER Ltd., 2022. http://dx.doi.org/10.37904/metal.2022.4495.

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Mangalagiu, Violeta, Dumitrela Diaconu, and Ionel Mangalagiu. "Quinoline - sulfonamide - complexes with antimicrobial activity." In Scientific seminar with international participation "New frontiers in natural product chemistry". Institute of Chemistry, Republic of Moldova, 2023. http://dx.doi.org/10.19261/nfnpc.2023.ab26.

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Quinoline-sulfonamide-complexes with variously metals, especially M2+, are a relatively new class of compounds with potential practical interest as fluorescent materials (having fotoluminiscent properties) and also as drugs (having a large variety of biological activities such as antibacterial, antifungal, antiprotozoals, etc.). The emphasis of this work was to obtain hybrid quinoline – sulfonamide - complexes with antimicrobial activity. The synthesis of the hybrid derivatives is direct and efficient, in two steps: acylation of variously amino-quinoline followed by metal complexation with dif
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Papadimitrakopoulos, Fotios, D. Laurence Thomsen III, and Keith A. Higginson. "Quinoline-based polymeric metal chelate light-emitting diodes." In Optical Science, Engineering and Instrumentation '97, edited by Zakya H. Kafafi. SPIE, 1997. http://dx.doi.org/10.1117/12.279326.

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Diaconu, Dumitrela, Violeta Mangalagiu, Dorina Amariucai-Mantu, Vasilichia Antoci, and Ionel Mangalagiu. "SIX-MEMBERED HETEROCYCLIC SULFONAMIDES: SYNTHESIS, CHARACTERISATION AND ANTIMICROBIAL PROPERTIES." In 23rd SGEM International Multidisciplinary Scientific GeoConference 2023. STEF92 Technology, 2023. http://dx.doi.org/10.5593/sgem2023v/6.2/s25.45.

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Sulfonamides are appropriate ligands for the preparation of coordination compounds with biological activity, as they possess bactericidal, antiviral, antidiabetic, and diuretic properties and some sulfonamide compounds are under clinical evaluation for cancer treatment. Metal complexes provide highly versatile platforms for drug design. Considering the biological potential of the quinoline nucleus, but also of the sulfonamide scaffold (especially antimicrobial), as well as that of the quinoline- sulfonamide combination we have decided to combine the two pharmacophore fragments. And at last, th
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Sawde, S. M., R. R. Patil, and S. V. Moharil. "Study of photoluminescence properties of trivalent metal ion (Al3+) coumarinolates doped with quinoline for PCLED application." In 3RD INTERNATIONAL CONFERENCE ON CONDENSED MATTER AND APPLIED PHYSICS (ICC-2019). AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0002688.

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Reports on the topic "Methyl quinoline"

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Bradshaw, Jerald S., Guoping Xue, Xian X. Zhang, Paul B. Savage, and Krzysztof E. Krakowiak. Bis-(quinolin-8-ylmethyl)-substituted Diaza-18-crown-6: Synthesis and Metal Ion Complexation Properties. Defense Technical Information Center, 2000. http://dx.doi.org/10.21236/ada375274.

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