Relevant bibliographies by topics / Quinolium

Contents

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

Academic literature on the topic 'Quinolium'

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

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Journal articles on the topic "Quinolium"

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R, GURUMURTHY, and KARUNAKARAN K. "A Comparative Study on the Kinetics of Oxidation of some Organic Sulphides by Quinolium Chlorochromate and Hexacyanoferrate(III)." Journal of Indian Chemical Society Vol. 72, May 1995 (1995): 349–51. https://doi.org/10.5281/zenodo.5904945.

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Department of Chemistry, Annamalai University, Annamalai Nagar-608 002 <em>Manusript received 23 September 1993, revised 6 December 1993, accepted 10 December 1993</em> A Comparative Study on the Kinetics of Oxidation of some Organic Sulphides by Quinolium Chlorochromate and Hexacyanoferrate(III)
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Kim, Tae Wan, Sang-Kug Lee, Min-Jong Song, Dong-Myung Shin, Young-Soo Kwon, and Dou-Yol Kang. "Thermal annealing effects of C22-Quinolium(TCNQ) Langmuir-Blodgett films." Synthetic Metals 71, no. 1-3 (1995): 2029–30. http://dx.doi.org/10.1016/0379-6779(94)03150-5.

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Son, Jung-Ho, Sem Raj Tamang, Jason C. Yarbrough, and James D. Hoefelmeyer. "Hydrolysis of 8-(pinacolboranyl)quinoline: where is the 8-quinolylboronic acid?" Zeitschrift für Naturforschung B 70, no. 11 (2015): 775–81. http://dx.doi.org/10.1515/znb-2015-0031.

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AbstractThe compound 8-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-quinoline was prepared and found to hydrolyze rapidly in air; however, the expected product (quinolin-8-yl)boronic acid was not observed. Instead, the (quinolinium-8-yl)trihydroxyborate zwitterion or an anhydride were observed depending on the conditions of hydrolysis. The two products are related to one another in the degree of hydration, and the two forms could be interconverted. Both hydrolysis products were structurally characterized. Additionally, a commercial sample of ‘8-quinolylboronic acid’ was actually found to be t
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Kim, Tae-Wan, Seung-Kyu Park, Dou-Yol Kang, Eon-Sik Hong, and Chul Park. "Anisotropic DC Electrical Conductivity and AC Response in C22-Quinolium (TCNQ) LB Films at Room Temperature." Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals 227, no. 1 (1993): 243–54. http://dx.doi.org/10.1080/10587259308030977.

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Kim, Tae Wan, Dong-Myung Shin, Il-Seok Song, Dou-Yol Kang, and Young-Soo Kwon. "Temperature-Dependent I-V Characteristics and Thermal Annealing Effects of C22-Quinolium(TCNQ) Langmuir-Blodgett Films." Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals 247, no. 1 (1994): 233–42. http://dx.doi.org/10.1080/10587259408039209.

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Sabo, T., D. Kut, M. Kut, M. Onysko, and V. Lendel. "TELLURO-INDUCED CYCLIZATION OF 2-ALLYLTHIOQUINOLINECARBALDEHYDE." Scientific Bulletin of the Uzhhorod University. Series «Chemistry» 46, no. 2 (2022): 74–79. http://dx.doi.org/10.24144/2414-0260.2021.2.74-79.

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It is known that thiazolopyrimidines with an exocyclic aryl tellurium moiety exhibit antimalarial activity against the deadliest strain of Plasmodium falciparum. For expanding the number of potentially biologically active compounds with an exocyclic aryl tellurium moiety, a study of tellurium-induced heterocyclization of 2-allylthioquinoline-3-carbaldehyde with p-methoxyphenylteltur trichloride was performed. The selection of this synton is motivated by the fact that quinoline derivatives are used as drugs in the treatment of malaria.&#x0D; The starting compound 2-allylthioquinoline-3-carbalde
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Kanta De, Surya. "Quinolium Dichromate Adsorbed on Alumina: A Mild, Convenient, and Inexpensive Reagent for Cleavage of C˭N Under Nonaqueous Conditions." Synthetic Communications 35, no. 20 (2005): 2641–44. http://dx.doi.org/10.1080/00397910500213047.

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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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Ghorab, Mostafa M., and Mansour S. Alsaid. "Anti-breast cancer activity of some novel quinoline derivatives." Acta Pharmaceutica 65, no. 3 (2015): 271–83. http://dx.doi.org/10.1515/acph-2015-0030.

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Abstract To discover new bioactive lead compounds for medicinal purposes, 2-cyano-3-(4-substituted)-N-(quinolin-3-yl) acrylamide derivatives 2–24, chromenes 25, 26 and benzochromenes 27, 28 were synthesized. The structures of the newly synthesized compounds were confirmed by elemental analyses, IR, 1H NMR and 13C NMR spectroscopies. In addition, the structure of compound 1 was confirmed through X-ray crystallography. All the newly synthesized compounds were evaluated for their cytotoxic activity against the breast cancer cell line MCF7. The corresponding 2-cyano-3-(4-hydroxy-3-methoxyphenyl)-N
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Bremner, JB, та W. Jaturonrusmee. "Manganese(III) Acetate-Induced Formation of a Fused, Chloro-Substituted β-Lactam Derivative From a Chloroacetamide". Australian Journal of Chemistry 43, № 8 (1990): 1461. http://dx.doi.org/10.1071/ch9901461.

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Reaction of 1-chloroacetyl-5-methoxy-2,3-dihydro-1H-dibenzo[de,h]quinoline (1) with manganese(III) acetate in acetic acid at 50° gave the novel fused spiro derivative 11-chloro-4-methoxy-1,2-dihydro-6H-azeto[2,1-f]dibenzo[de,h]quinoline-6,12(11H)-dione (6) in 21% yield, together with 5-methoxy-7H-dibenzo[de,h]quinolin-7-one (3), 5-methoxy-2,3-dihydro-7H-dibenzo[de,h]quinolin-7-one (4), and 1- chloroacetyl-5-methoxy-2,3-dihydro-1H-dibenzo[de,h]-quinolin-7-yl ethanoate (5) in 1, 3 and 44% yields respectively. Compound (5) was shown to be a precursor of (3), (4) and (6).
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Dissertations / Theses on the topic "Quinolium"

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Correia, Fábio Conte. "Síntese e caracterização de polímeros contendo 9,9-dioctilfluoreno e 8-oxioctilquinolina para utilização como camada emissora de PLEDs." Universidade de São Paulo, 2013. http://www.teses.usp.br/teses/disponiveis/3/3133/tde-11072014-115535/.

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Utilizando a reação de acoplamento de Suzuki, novos polímeros e copolímeros semicondutores com elevado potencial para a fabricação de PLEDs foram sintetizados, tendo como finalidade unir em uma única camada emissiva, na forma de copolímeros ou na forma de blendas, materiais com propriedades transportadoras e injetoras de elétrons; grupos quinolina associados a materiais com elevadas propriedades de emissão de luz contendo grupos fluoreno. Esses copolímeros sintetizados, todos ainda não descritos na literatura ou em patentes, apresentaram rendimentos acima de 70% e rendimentos quânticos de foto
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Madureira, Luana Barreto. "Adsorção de quinolina em sílica-alumina a partir de soluções com n-hexadecano por calorimétrica: estudo da cinética e da isoterma." Universidade do Estado do Rio de Janeiro, 2014. http://www.bdtd.uerj.br/tde_busca/arquivo.php?codArquivo=7438.

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As legislações ambientais estão cada vez mais severas em relação à quantidade de compostos sulfurados eliminada na atmosfera pela queima de combustíveis fósseis. Os processos de adsorção têm se destacado como uma alternativa promissora na remoção de sulfurados presentes em combustíveis. Nos estudos de adsorção, ensaios de cinética e isoterma usando banhos agitados são frequentemente utilizados na avaliação do desempenho dos adsorventes na remoção desejada. Apesar de úteis, tais ensaios apresentam algumas limitações quando os sistemas analisados envolvem elevadas relações entre a concentração i
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Abner, Erik 1986. "Identification of HIV-1 reactivating quinoline compounds as bromodomain inhibitors." Doctoral thesis, Universitat Pompeu Fabra, 2016. http://hdl.handle.net/10803/565528.

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Tras la infección por VIH-1, el establecimiento de un depósito de células T en reposo infectadas latentemente con VIH impide la erradicación del virus en pacientes. Para lograr la erradicación, la terapia retroviral existente debe combinarse con medicamentos que reactiven los virus latentes. Previamente, nuestro grupo describió un nuevo compuesto químico, MMQO (8-metoxi-6-metilquinolin-4-ol) que es capaz de reactivar la transcripción viral a través de un mecanismo desconocido. El objetivo de este proyecto fue identificar los proteínas que interaccionan con MMQO e investigar su papel en la reac
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Arif, Arif Saleem. "Separation of quinoline and iso-quinoline by dissociation extraction." Thesis, Teesside University, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.410847.

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Barr, Stephen Alexander. "Quinoline alkaloids : synthesis and stereochemistry." Thesis, Queen's University Belfast, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.333796.

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Ferreira, Maria Eugênia de Oliveira. "Adsorção de compostos nitrogenados utilizando carvão ativado." Universidade Federal de Goiás, 2017. http://repositorio.bc.ufg.br/tede/handle/tede/8749.

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Submitted by Marlene Santos (marlene.bc.ufg@gmail.com) on 2018-07-27T18:43:45Z No. of bitstreams: 2 Dissertação - Maria Eugênia de Oliveira Ferreira - 2017.pdf: 2295850 bytes, checksum: 937ef23483ab6e46d51253d73c4e2ef2 (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5)<br>Approved for entry into archive by Luciana Ferreira (lucgeral@gmail.com) on 2018-07-30T14:07:22Z (GMT) No. of bitstreams: 2 Dissertação - Maria Eugênia de Oliveira Ferreira - 2017.pdf: 2295850 bytes, checksum: 937ef23483ab6e46d51253d73c4e2ef2 (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e980
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Ajaka, Camille Daher. "Catalytic hydrodenitrogenation of pyridine and quinoline." Thesis, University of Ottawa (Canada), 1991. http://hdl.handle.net/10393/5877.

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The reaction networks and the kinetics of the vapor phase catalytic hydro-denitrogenation (HDN) of two model nitrogen-containing heterocyclic compounds, pyridine, quinoline and their mixture, were studied in a bench scale continuous flow, fixed-bed catalytic reactor. The catalyst used in this study was presulfided commercial Ni-Mo/$\rm Al\sb2O\sb3$ (Shell Catalyst 424). The results indicate that the impact of the process variables on the conversion, yield, and selectivity of the HDN reactions is in the following decreasing order: $T>W/F>\bar R.$ The initial aromatic ring saturation reactions o
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Klaas, Phindile Jonathan. "Novel approaches to the synthesis of quinoline derivatives." Thesis, Rhodes University, 2001. http://hdl.handle.net/10962/d1004751.

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The investigation has been concerned with the application of the Baylis-Hillman methodology to the synthesis of quinoline derivatives. An extensive range of novel Baylis-Hillman products has been prepared, typically in moderate to excellent yields, by condensing 2-nitrobenzaldehyde derivatives with various vinyl ketones and acrylic esters in the presence of diazabicyclo[2.2.2]octane (DABCO). Reduction of the nitro group in the Baylis-Hillman products was effected by catalytic hydrogenation in ethanol using a 10% palladium-on-carbon catalyst to afford quinoline, quinoline-N-oxide and quinolone
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Carvajal-Figueroa, Maria Teresa 1959. "Solubility of quinoline in aqueous systems: Effect of pH and ionic strength." Thesis, The University of Arizona, 1989. http://hdl.handle.net/10150/291584.

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Nitrogen-heterocyclic compounds are commonly found in gas waste and coal cleaning residue. Within this general compound class, quinoline is especially important because it has the potential to induce liver carcinoma and it also has a high solubility in water. The pH-solubility profile of quinoline was determined in citrate-phosphate buffer at different ionic strengths. The pKa was observed to change with ionic strength. The intrinsic solubility is always reported as a constant. However, in this study the intrinsic solubility was observed to vary with ionic strength. The solubility of quinoline
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Apple, Ian Allan. "The alkaline peroxide oxidation of quinolinium salts." Thesis, University of Sunderland, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.288879.

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Books on the topic "Quinolium"

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Rutherford, Mary Jean. Dimeric indole and quinoline alkaloids. The author], 1985.

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Neville, Charles Frederick. The synthesis and biosynthesis of quinoline alkaloids. The Author], 1989.

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Greer, Robert James. Studies in the synthesis of quinoline alkaloids. The Author), 1987.

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Giles, Janice S. In vitro efficacy of six antibiotics and plasma concentrations of two quinolines in Atlantic salmon (salmon salari). University of Prince Edward Island, 1992.

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Giles, Janice S. In vitro efficacy of six antibiotics and plasma concentrations of two quinolines in Atlantic salmon (salmon salari). National Library of Canada, 1992.

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Edlund, Charlotta. Ecological aspects of new quinolones: Impact on human oropharyngeal and gastrointestinal microflora. Kongl. Karolinska Medico Chirurgiska Institutet, 1989.

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Ronne, Erik. Synthesis of imidazoazaarenes. Swedish University of Agricultural Sciences, Dept. of Chemistry, 1994.

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Jones, Dewitt Owen. Catalysis of Hydrogen Peroxide in Quinoline Solutions. Creative Media Partners, LLC, 2023.

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Di, Kaiying. Interactions between substrates and starved subsurface bacteria in a dual-bacteria/dual-contaminant system. 1993.

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Zhang, Jinying. Effects of quinolinate and nitro-, or thio- substituted analogs of quinolinate on glutamate recepter-mediated neurotoxicity in cerebellar granule cell cultures. 1998.

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Book chapters on the topic "Quinolium"

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of quinolium diaquadicitratodiferrate(III) tetrahydrate." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 1. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62478-4_450.

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Lide, David R. "Quinoline." In Handbook of Organic Solvents. CRC Press, 2024. http://dx.doi.org/10.1201/9781003575191-419.

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Greenhill, John V. "Quinoline Aldehydes." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470187043.ch1.

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Greenhill, John V. "Quinoline Ketones." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470187043.ch2.

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Méndeza, Leonor Y. Vargas, Vladimir V. Kouznetsov, Nüket Öcal, Zuhal Turgut, and Çiğdem Yolaçan. "Convenient Route to Quinoline-Tetrahydroquinolines from Quinoline-Carboxaldehydes." In Biodiversity. Springer US, 2002. http://dx.doi.org/10.1007/978-1-4419-9242-0_52.

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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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Li, Jie Jack. "Pfitzinger quinoline synthesis." In Name Reactions. Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05336-2_232.

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Li, Jie Jack. "Skraup quinoline synthesis." In Name Reactions. Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05336-2_278.

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Li, Jie Jack. "Combes quinoline synthesis." In Name Reactions. Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05336-2_64.

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Vogt, J. "714 C9H7N Quinoline." In Asymmetric Top Molecules. Part 3. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-14145-4_136.

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Conference papers on the topic "Quinolium"

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Vera, Jose, William Durnie, Ashwini Chandra, Kevin Ralston, and Richard Woollam. "On the Adsorption Properties of Non-Surfactant Corrosion Inhibitors: Pyridine, Quinoline and Acridine." In CORROSION 2021. AMPP, 2021. https://doi.org/10.5006/c2021-16686.

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Abstract Most of the carbon dioxide (CO2) corrosion inhibition work published has been based on constituents that behave as surfactants (e.g., quaternary amines and imidazolines). For these compounds, a relationship has been found between the concentration for maximum efficiency and the critical micelle concentration (CMC) and, more recently, with the concentration of maximum adsorption (CMA) on platinum. This paper shows how the methodology developed to characterize inhibitors based on their CMA values is still applicable to non-surfactant corrosion inhibitors, which would not show a CMC. The
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Schmitt, G., C. Bosch, H. Bauer, and M. Mueller. "Modelling the Drag Reducing Effect of CO2 Corrosion Inhibitors." In CORROSION 2000. NACE International, 2000. https://doi.org/10.5006/c2000-00002.

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Abstract The drag reducing effect of corrosion inhibitors was measured at a microelectrode array incorporated flush into a surface impinged with a submerged jet. The measurements were performed under mass transport control with the hexacyanoferrate(II)/(III) redox system. N-(2-methylenenaphthyl)-quinolinium bromide (MNQB) yielded a drag reducing factor of 0.5 at concentrations of 0.5 mM, and trimethylammonium chlorides with C12-18 chain yield factors of 0.2 above their critical micelle concentration. Critical inhibitor concentrations from electrochemical measurements match very well with resul
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Jauhari, Smita, and Bhupendra Mistry. "“Study of the Inhibitive Effect of Novel Quinoline Schiff Base on Corrosion of Mild Steel in HCl Solution”." In CORROSION 2013. NACE International, 2013. https://doi.org/10.5006/c2013-02326.

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Abstract Schiff base 4-Chloro-N-[(2-chloroquinolin-3-yl)methylene]aniline was synthesized, and its inhibitive effect for mild steel in 1M HCl solution was investigated by weight loss measurement and electrochemical tests.From the weight loss measurements and electrochemical tests, it was observed that the inhibition efficiency increases with the increase in the Schiff base concentration and reaches a maximum at the optimum concentration. This is further confirmed by the decrease in corrosion rate. It is found that the system follows Langmuir adsorption isotherm.
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Yang, Zhen, Yefei Wang, Fengtao Zhan, et al. "Investigation of High-efficient Acidizing Inhibitors: Structure and Anti-corrosion Performance of Novel Indolizine Derivatives." In CORROSION 2019. NACE International, 2019. https://doi.org/10.5006/c2019-12744.

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Abstract The novel indolizine derivative inhibitor for acidizing shows an effective corrosion inhibition without the synergism of propargyl alcohol. The inhibitive indolizine derivatives were generated from BQC (Benzyl Quinolinium Chloride, a commonly used key compound in acidizing inhibitor) via a moderate 1,3-dipolar cycloaddition mechanism. High Resolution Mass Spectrometry (HRMS) and NMR were used to confirm the detailed chemical structure. The inhibition of two indolizine derivatives in 15 wt.% HCl for N80 steel were studied by weight loss measurement and electrochemical analysis. Without
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Kopecky, Sarah E. "Investigation of Substituent Effects on the Corrosion Inhibition of Pyridine Derivatives with Acetylenic Alcohols on Steel in Acid Media." In CORROSION 2015. NACE International, 2015. https://doi.org/10.5006/c2015-05569.

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Abstract The corrosion inhibition of substituted pyridine derivatives and quaternized pyridines in the presence and absence of acetylenic alcohol synergists is reported. Electrochemical Frequency Modulation (EFM) was used as a method of monitoring corrosion rates of steel in acidic environments. Early stage pitting was evaluated via scanning electron microscope (SEM) for comparison of measured corrosion rates to observed pit formation. EFM was found to be a reliable and accurate method of monitoring general corrosion rates over time, and causality factor data was found to depend heavily on the
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Yang, Zhen, Yefei Wang, Matjaž Finšgar, Jiajia Wu, and Wengang Ding. "Novel High-Efficient Key Component of Steel Corrosion Inhibitors Formulation for Acidification: Indolizine Derivatives of the Conventional N-Heterocyclic Quaternary Ammonium Salts." In SPE International Conference on Oilfield Chemistry. SPE, 2023. http://dx.doi.org/10.2118/213814-ms.

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Abstract Acidizing, the widely used technique for well stimulation, requires a great consumption of effective Corrosion Inhibitors (CIs), due to the severe and fast corrosion of metallic equipment caused by strong hot acid as soon as the acidizing fluids are pumping down to reservoir. This paper presents a new concept of indolizine derivative inhibitors with remarkable inhibition effectiveness for steel under acidizing condition, which will reduce the cost and environmental burden of acidizing CIs significantly. Indolizine derivatives of several quinolinium salts (serves as main component of c
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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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Zbancioc, Gheorghita, Costel Moldoveanu, and Ionel I. Mangalagiu. "Syntheses of new benzoquinoline derivatives with anticancer activity." In Conferința științifică națională cu participare internațională "Integrare prin cercetare și inovare", dedicată Zilei Internaționale a Științei pentru Pace și Dezvoltare. Moldova State University, 2025. https://doi.org/10.59295/spd2024n.92.

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This work synthesized various novel benzo[c]quinoline compounds, detailed their structural features, and examined their anticancer activity in vitro. First, the nitrogen atom in benzo[c]quinoline is quaternized, and the in situ-formed ylide is then subjected to a [3+2] dipolar cycloaddition reaction. A detailed investigation was conducted to determine how successful traditional thermal heating (TH) synthesis was in comparison to microwave (MW) and ultrasonic (US) irradiation. FTIR, HRMS, and NMR were the three spectral techniques that were used to prove the structure of all the obtained compou
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Musiol, Robert, Josef Jampilek, Katarina Kralova, et al. "New Quinoline Derivatives Possessing Herbicidal Activity." In The 9th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2005. http://dx.doi.org/10.3390/ecsoc-9-01508.

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10

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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Abstract:
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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Reports on the topic "Quinolium"

1

Steele, W., and R. Chirico. Thermodynamics of the hydrodenitrogenation of quinoline. Office of Scientific and Technical Information (OSTI), 1990. http://dx.doi.org/10.2172/6958305.

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2

Gunsaru, Bornface. Simplified Reversed Chloroquines to Overcome Malaria Resistance to Quinoline-based Drugs. Portland State University Library, 2000. http://dx.doi.org/10.15760/etd.400.

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3

Wang, Hong, Eric Wolfe, Edgar Lara-Curzio, Marco Martinez, and Tracie Lowe. Study on Electrostatic Separation of Quinoline Insolubles from Coal Tar Pitch. Office of Scientific and Technical Information (OSTI), 2023. http://dx.doi.org/10.2172/1960688.

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4

Steele, W., S. Knipmeyer, and R. Chirico. Critical property and high-temperature heat-capacity measurements on quinoline and 5,6,7,8-tetrahydroquinoline. Office of Scientific and Technical Information (OSTI), 1990. http://dx.doi.org/10.2172/6957875.

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5

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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