Quinolin (Vietnamese Wikipedia)

Analysis of information sources in references of the Wikipedia article "Quinolin" in Vietnamese language version.

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archive.org

books.google.com

  • F. F. Runge (1834) "Ueber einige Produkte der Steinkohlendestillation" (On some products of coal distillation), Annalen der Physik und Chemie, 31 (5): 65–78; see especially p. 68: "3. Leukol oder Weissöl" (3. White oil [in Greek] or white oil [in German]). From p. 68: "Diese dritte Basis habe ich Leukol oder Weissöl genannt, weil sie keine farbigen Reactionen zeigt." (This third base I've named leukol or white oil because it shows no color reactions.)

chemicalland21.com

doi.org

  • Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. pp. 4, 211. doi:10.1039/9781849733069-FP001. ISBN 978-0-85404-182-4.The name ‘quinoline’ is a retained name that is preferred to the alternative systematic fusion names ‘1-benzopyridine’ or ‘benzo[b]pyridine’.
  • Gerd Collin; Hartmut Höke. “Quinoline and Isoquinoline”. Bách khoa toàn thư Ullmann về Hóa chất công nghiệp. Weinheim: Wiley-VCH. doi:10.1002/14356007.a22_465. Lỗi chú thích: Thẻ <ref> không hợp lệ: tên “Hoke” được định rõ nhiều lần, mỗi lần có nội dung khác
  • O'Loughlin, Edward J.; Kehrmeyer, Staci R.; Sims, Gerald K. (1996). “Isolation, characterization, and substrate utilization of a quinoline-degrading bacterium”. International Biodeterioration & Biodegradation. 38 (2): 107. doi:10.1016/S0964-8305(96)00032-7.
  • GRIBBLE, Gordon W.; HEALD, Peter W. (1975). “Reactions of Sodium Borohydride in Acidic Media; III. Reduction and Alkylation of Quinoline and Isoquinoline with Carboxylic Acids”. Synthesis. 1975 (10): 650–652. doi:10.1055/s-1975-23871. ISSN 0039-7881.

hathitrust.org

babel.hathitrust.org

wikisource.org

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worldcat.org