Relevant bibliographies by topics / Nitroquinolines

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  1. Journal articles

Academic literature on the topic 'Nitroquinolines'

Author: Grafiati
Published: 4 June 2021
Last updated: 10 February 2022

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Journal articles on the topic "Nitroquinolines"

1

Szpakiewicz, Barbara, and Maria Grzegożek. "Vicarious nucleophilic amination of nitroquinolines with 4-amino-1,2,4-triazole." Canadian Journal of Chemistry 86, no. 7 (2008): 682–85. http://dx.doi.org/10.1139/v08-051.

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3-, 5-, 6-, 7- and 8-Nitroquinolines react with 4-amino-1,2,4-triazole in basic medium (potassium tert-butoxide-dimethyl sulfoxide) giving amino products of the vicarious nucleophilic substitution (VNS) of hydrogen, predominantly at ortho position to the nitro group, except 8-nitroquinoline, which reacts at para position. Additionally, furazano[3,4-f]- and furazano[3,4-h]quinoline were obtained in the case of 5- and 8- nitroquinoline, respectively. 2-Nitroquinoline was aminated to 2-quinolino(1,2,4-triazol-4-yl)amine in these conditions.Key words: nitroquinolines, vicarious nucleophilic substi
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2

Wantulok, Jakub, Daniel Swoboda, Jacek E. Nycz, et al. "Direct Amination of Nitroquinoline Derivatives via Nucleophilic Displacement of Aromatic Hydrogen." Molecules 26, no. 7 (2021): 1857. http://dx.doi.org/10.3390/molecules26071857.

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The vicarious nucleophilic substitution of hydrogen (VNS) reaction in electron-deficient nitroquinolines was studied. Properties of all new products have been characterized by several techniques: MS, HRMS, FTIR, GC-MS, electronic absorption spectroscopy, and multinuclear NMR. The structures of 4-chloro-8-nitroquinoline, 8-(tert-butyl)-2-methyl-5-nitroquinoline, 9-(8-nitroquinolin-7-yl)-9H-carbazole and (Z)-7-(9H-carbazol-9-yl)-8-(hydroxyimino)quinolin-5(8H)-one were determined by single-crystal X-ray diffraction measurements. The 9-(8-nitroquinolin-7-yl)-9H-carbazole and (Z)-7-(9H-carbazol-9-y
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3

Woźniak, Marian, and Maria Grzegożek. "Oxidative Methylamination of Nitroquinolines." Liebigs Annalen der Chemie 1993, no. 8 (1993): 823–29. http://dx.doi.org/10.1002/jlac.1993199301130.

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4

WOZNIAK, M., and M. GRZEGOZEK. "ChemInform Abstract: Oxidative Methylamination of Nitroquinolines." ChemInform 24, no. 48 (2010): no. http://dx.doi.org/10.1002/chin.199348089.

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5

Skolyapova, Alexandrina D., Galina A. Selivanova, Evgeny V. Tretyakov, Irina Yu Bagryanskaya, and Vitalij D. Shteingarts. "Synthesis of polyfluorinated aminoquinolines via nitroquinolines." Journal of Fluorine Chemistry 211 (July 2018): 14–23. http://dx.doi.org/10.1016/j.jfluchem.2018.04.006.

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6

Luque-Agudo, V., José M. Padrón, E. Román, J. A. Serrano, and M. V. Gil. "Antiproliferative activity of new 2-glyco-3-nitro-1,2-dihydroquinolines and quinolines synthesized under solventless conditions promoted by neutral alumina." New Journal of Chemistry 42, no. 22 (2018): 18342–47. http://dx.doi.org/10.1039/c8nj03372b.

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This paper describes the syntheses of new 2-glyco-3-nitro-1,2-dihydroquinolines and 2-glyco-3-nitroquinolines by one-pot aza-Michael–Henry-dehydration reactions using green procedures, as well as the evaluation of their antiproliferative activity.
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7

Glushkov, R. G., and N. K. Davydova. "Chemistry of 3-nitroquinolines and their derivatives (review)." Pharmaceutical Chemistry Journal 26, no. 4 (1992): 325–37. http://dx.doi.org/10.1007/bf00773165.

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8

Fabian, Walter. "Zur Interpretation des Substituenteneinflusses auf das UV-spektroskopische Verhalten von Chinolinderivaten." Zeitschrift für Naturforschung A 40, no. 7 (1985): 719–25. http://dx.doi.org/10.1515/zna-1985-0712.

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The results of PPP calculations on the seven isomeric amino- as well as nitroquinolines (chosen as models for donator and acceptor substituted derivatives) are analyzed by means of configuration analysis. Based on these analyses the characteristic dependence of the UV spectra of these compounds on the position and nature of the substituent is interpreted and verified using a simplified molecules-in-molecule calculation.
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9

Grzegożek, Maria. "Vicarious nucleophilic amination of nitroquinolines by 1,1,1-trimethylhydrazinium iodide." Journal of Heterocyclic Chemistry 45, no. 6 (2008): 1879–82. http://dx.doi.org/10.1002/jhet.5570450652.

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10

Tondys, Hanna, Henk C. van der Plas, and Marian Woźniak. "On the chichibabin amination of quinoline and some nitroquinolines." Journal of Heterocyclic Chemistry 22, no. 2 (1985): 353–55. http://dx.doi.org/10.1002/jhet.5570220226.

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