References analysis of the Wikipedia article "Chinolin" in the German version

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O. Eckstein: Ueber Chinolin-chlorhydrat und die Einwirkung von Säurechloriden auf Chinolin. In: Chem. Ber., 1906, 39, S. 2135–2138; doi:10.1002/cber.190603902173.

A. D. Buckingham, J. Y. H. Chau, H. C. Freeman, R. J. W. Le Fèvre, D. A. A. S. Narayana Rao, J. Tardif: The dipole moments of pyridine, quinoline, and isoquinoline as vapours and as solutes. In: J. Chem. Soc., 1956, S. 1405–1411; doi:10.1039/JR9560001405.

W. H. F. Sasse: Synthetical applications of activated metal catalysts. Part VIII. The action of degassed Raney nickel on quinoline and some of its derivatives. In: J. Chem. Soc., 1960, S. 526–533; doi:10.1039/JR9600000526.

W. V. Steele, D. G. Archer, R. D. Chirico, W. B. Collier, I. A. Hossenlopp, A. Nguyen, N. K. Smith, B. E. Gammon: The thermodynamic properties of quinoline and isoquinoline. In: J. Chem. Thermodynamics, 1988, S. 1233–1264; doi:10.1016/0021-9614(88)90161-9.

Ch. Gerhardt: Untersuchungen über die organischen Basen. In: Annalen der Chemie und Pharmacie, 1942, 42, S. 310–313; doi:10.1002/jlac.18420420310.

Ch. Gerhardt: Untersuchungen über die chemische Classification der organischen Substanzen. In: J. Prakt. Chem., 1843, 28, S. 65–100; doi:10.1002/prac.18430280112.

Monatsbericht: Chinolin. In: Archiv der Pharmazie, 1882, 20, S. 50–73; doi:10.1002/ardp.18822200109.

Paul Rabe: Untersuchungen in der Pyridin- und Chinolinreihe. In: J. Prakt. Chem., 1938, 151, S. 65–81; doi:10.1002/prac.19381510203.

W. Königs: Oxydationsprodukte des Cinchonins. In: Chem. Ber., 1879, 12, S. 79–101; doi:10.1002/cber.18790120130.

S. Hoogewerff, W. A. van Dorp: Sur la quinoléine du goudron de houille et des alcaloïdes du quinquina, et sur leur oxydation au moyen du permanganate de potassium. In: Rec. Trav. Chim., 1882, 1, S. 1–17; doi:10.1002/recl.18820010501.

B. Aronheim: Synthese des Naphthalin. In: Chem. Ber., 1873, 6, S. 67–68; doi:10.1002/cber.18730060125.

W. Koenigs: Synthese des Chinolins aus Allylanilin. In: Chem. Ber., 1879, 12, S. 453; doi:10.1002/cber.187901201128.

Z. H. Skraup: Eine Synthese des Chinolins. In: Chem. Ber., 1880, 13, S. 2086–2087; doi:10.1002/cber.188001302195.

O. Doebner, W. v. Miller: Ueber eine dem Chinolin homologe Base. In: Chem. Ber., 1881, 14, S. 2812–2817; doi:10.1002/cber.188101402258.

F. W. Bergstrom, Heterocyclic Nitrogen Compounds. Part IIA. Hexacyclic Compounds: Pyridine, Quinoline, and Isoquinoline. In: Chem. Rev., 1944, 35, S. 77–277; doi:10.1021/cr60111a001.

A. Shaabani, E. Soleimani, Z. Badri: Triflouroacetic Acid as an Efficient Catalyst for the Synthesis of Quinoline. In: Synth. Commun., 2007, 37, S. 629–635; doi:10.1080/00397910601055230.

C.-S. Jia, Z. Zhang, S.-J. Tu, G.-W. Wang: Rapid and efficient synthesis of poly-substituted quinolines assisted by p-toluene sulphonic acid under solvent-free conditions: comparative study of microwave irradiation versus conventional heating. In: Org. Biomol. Chem., 2006, 4, S. 104–110; doi:10.1039/b513721g.

J. Wu, H.-G. Xia, K. Gao: Molecular iodine: a highly efficient catalyst in the synthesis of quinolines via Friedländer annulation. In: Org. Biomol. Chem., 2006, 4, S. 126–129; doi:10.1039/b514635f.

R. Varala, R. Enugala, S. R. Adapa: Efficient and Rapid Friedlander Synthesis of Functionalized Quinolines Catalyzed by Neodymium(III) Nitrate Hexahydrate. In: Synthesis, 2006, S. 3825–3830; doi:10.1055/s-2006-950296.

R. H. Manske: The Chemistry of Quinolines. In: Chem. Rev., 1942, 30, S. 113–144; doi:10.1021/cr60095a006.

V. V. Kouznetsov, L. Y. V. Méndez, L. Y. V. Gómez: Recent Progress in the Synthesis of Quinolines. In: Curr. Org. Chem., 2005, 9, S. 141–161; doi:10.1002/chin.200516245.

R. H. Reitsema: The Chemistry of 4-Hydroxyquinolines. In: Chem. Rev., 1948, 43, S. 43–68; doi:10.1021/cr60134a002.

R. Camps: Synthese von alpha- und gamma-Oxychinolinen. In: Chem. Ber., 1899, 22, S. 3228–3234; doi:10.1002/cber.18990320389.

L. Knorr: Synthetische Versuche mit dem Acetessigester. In: Liebigs Ann., 1886, 236, S. 69–115; doi:10.1002/jlac.18862360105.

R. G. Gould, W. A. Jacobs: The Synthesis of Certain Substituted Quinolines and 5,6-Benzoquinolines. In: J. Am. Chem. Soc., 1939, 61, S. 2890–2895; doi:10.1021/ja01265a088.

J. E. Davies, A. D. Bond: Quinoline. In: Acta Cryst., 2001, E57, S. o947–o949; doi:10.1107/S1600536801014891.

M. W. Austin, J. H. Ridd: The kinetics and mechanism of heteroaromatic nitration. Part I. Quinoline. In: J. Chem. Soc., 1963, S. 4204–4210; doi:10.1039/JR9630004204.

G. E. McCasland: The Preparation of 8-Qinolinesulfonic acid. In: J. Org. Chem., 1946, 11, S. 277–280; doi:10.1021/jo01173a010.

J. L. Butler, M. Gordon: A reinvestigation of known bromination reactions of quinoline. In: J. Heterocycl. Chem., 1975, 12, S. 1015–1020; doi:10.1002/jhet.5570120539.

T. J. Kress, S. M. Constantino: Selective brominations in nitrobenzene. A convenient synthesis of 3-brornoquinoline, 4-bromoisoquinoline, and 4-phenyl-5-bromopyrimidine. In: J. Heterocycl. Chem., 1973, 10, S. 409–410; doi:10.1002/jhet.5570100326.

H. van der Plas: Oxidative Amino-Dehydrogenation of Azines. In: Adv. Heterocycl. Chem., 2004, 86, S. 1–40; doi:10.1016/S0065-2725(03)86001-4.

J. A. Zoltewicz, L. S. Helmick, T. M. Oestreich, R. W. King, P. E. Kandetzki: Addition of amide ion to isoquinoline and quinoline in liquid ammonia. Nuclear magnetic resonance spectra of anionic σ-complexes. In: J. Org. Chem., 1973, 38, S. 1947–1949; doi:10.1021/jo00950a036.

T. J. Geissmann, M. J. Schlatter, I. D. Webb, J. D. Roberts: The Synthesis of some Intermediates for the Use in the Preparation of Analogs of Salicylaldehyde ethylenediimine cobalt ("Salcomine"). In: J. Org. Chem., 1946, 11, S. 741–750; doi:10.1021/jo01176a015.

M. Ishikura, T. Mano, I. Oda, M. Terashima: An Alternative Synthesis of Dialkylpyridylboranes. In: Heterocycles, 1984, S. 4271–4274; doi:10.3987/R-1984-11-2471.

H. Gilman, T. Soddy: Notes - Some Organolithium Compounds of Quinoline and 2-Phenylquinoline. In: J. Org. Chem., 1958, 23, S. 1584–1585; doi:10.1021/jo01104a627.

J. B. Wommack, T. G. Barbee Jr., D. J. Thoennes, M. A. McDonald, D. E. Pearson: The synthesis of quinoline- and isoquinolinecarboxaldehydes. In: J. Heterocycl. Chem, 1969, 6, S. 243–245; doi:10.1002/jhet.5570060217.

J. Meisenheimer: Über Pyridin-, Chinolin- und Isochinolin-N-oxyd. In: Ber. Dtsch. Chem. Ges., 1926, 59, S. 1848–1853; doi:10.1002/cber.19260590828.

C. F. Koelsch, A. F. Steinhauer: Synthesis, Nitration, and Oxidation of 3-Azafluoranthene. In: J. Org. Chem., 1953, 18, S. 1516–1522; doi:10.1021/jo50017a010.

J. C. Cochran, W. F. Little: Electrolytic Oxidation of Some Substituted Quinolines to Quinolinic Acids and Acylations with Substituted Quinolinic Anhydrides. In: J. Org. Chem., 1961, 21, S. 808–811; doi:10.1021/jo01062a039.

C. O’Murchu: Ozonolysis of Quinolines: A Versatile Synthesis of Polyfunctional Pyridines. In: Synthesis, 1989, 11, S. 880–882; doi:10.1055/s-1989-27423.

G. R. Girard, W. E. Bondinell, L. M. Hillegass, K. G. Holden, R. G. Pendleton, I. Uzinskas: Tetrahydro thiadiazolo isoquinolines: synthesis and inhibition of phenylethanolamine-N-methyltransferase. In: J. Med. Chem., 1989, 32, S. 1566–1571; doi:10.1021/jm00127a027.

B. C. Ranua, U. Jana, A. Sarkara: Regioselective Reduction of Quinolines and Related Systems to 1,2,3,4-Tetrahydro Derivatives with Zinc Borohydride. In: Synth. Commun., 1998, 28, S. 485–492; doi:10.1080/00397919808005103.

G. L. Patrick: Synthesis of (±)-[4a^α,4b^β,10b^β,12a^α]-9-halogeno-2-methyl-1,2,3,4,4a,4b,5,6,10b,11,12,12a-dodecahydronaphtho[2,1-f]isoquinolines. In: J. Chem. Soc., Perkin Trans. 1, 1995, S. 1273–1279; doi:10.1039/P19950001273.

E. A. Braude, J. Hannah, Sir R. Linstead: Hydrogen transfer. Part XVI. Dihydrides of nitrogenous heterocycles as hydrogen donors. In: J. Chem. Soc., 1960, S. 3249–3257; doi:10.1039/JR9600003249.

Arthur Birch, P. G. Lehmann: 1,4-Dihydrochinolin. In: Tetrahedron Lett., 1974, 15, S. 2395–2396; doi:10.1016/S0040-4039(01)92265-8.

N. N. Woroshtzow, J. M. Kogan: Über die Wirkung von schwefliger Säure und ihren Salzen auf Chinolin-Derivate. In: Ber. Dtsch. Chem. Ges., 1930, S. 2354–2362; doi:10.1002/cber.19300630878.

S. Hoogewerff, W. A. van Dorp: Ueber die Oxydation von Chinolin vermittelst Kaliumpermanganat. In: Chem. Ber., 1879, 12, S. 747–748; doi:10.1002/cber.187901201208.

H. Lindlar, R. Dubuis: Palladium Catalyst for Partial Reduction of Acetylenes In: Organic Syntheses. 46, 1966, S. 89, doi:10.15227/orgsyn.046.0089; Coll. Vol. 5, 1973, S. 880 (PDF).

H. Lindlar: Ein neuer Katalysator für selektive Hydrierungen. In: Helv. Chim. Acta, 1952, 35, S. 446–450; doi:10.1002/hlca.19520350205.

E. J. LaVoie, A. Shigematsu, E. A. Adams, J. Rigotty, D. Hoffmann: Tumor-initiating activity of quinoline and methylated quinolines on the skin of SENCAR mice. In: Cancer Lett., 1984, 22, S. 269–273; doi:10.1016/0304-3835(84)90162-9; PMID 6324986.

H. Tschammler, H. Krischai: Chinolin-m-Kresol, ein stark negatives System. In: Monatsh. Chem., 1951, 82, S. 259–270; doi:10.1007/BF00899511.

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K. Hirao, Y. Shinohara, H. Tsuda, S. Fukushima, M. Takahashi, N. Ito: Carcinogenic Activity of Quinoline on Rat Liver. In: Cancer Res., 1976, 36, S. 329–335; PMID 177193 (Volltextzugriff; PDF; 1,3 MB).

Y. Shinohara, T. Ogiso, M. Hananouchi, K. Nakanishi, T. Yoshimura, N. Ito: Effect of various Factors on the Induction of Liver Tumors in Animals by Quinoline. In: GANN, 1977, 68, S. 785–796; PMID 598648.

J. T. Smith, R. N. Williams: Studies in detoxication. 65. The metabolism of quinoline. New metabolites of quinoline, with observations on the metabolism of 3-, 5- and 6-hydroxyquinoline and 2:4-dihydroxyquinoline. In: Biochem. J., 1955, 60, S. 284–290; PMC 1215695 (freier Volltext).

Chinolin (German Wikipedia)

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