Хінолін (Ukrainian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Хінолін" in Ukrainian language version.

refsWebsite

Global rank Ukrainian rank

31doi.org

2^nd place

4^th place

2web.archive.org

1^st place

2wikidata.org

43^rd place

134^th place

1merck.de

low place

9,961^st place

1orgsynth.org

low place

1nii.ac.jp

304^th place

low place

doi.org

dx.doi.org

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, 1405—1411; DOI:10.1039/JR9560001405.
Z. H. Skraup: Eine Synthese des Chinolins, in: Chem. Ber. 1880, 13, 2086—2087; DOI:10.1002/cber.188001302195.
A. Shaabani, E. Soleimani, Z. Badri: Triflouroacetic Acid as an Efficient Catalyst for the Synthesis of Quinoline, in: Synth. Commun. 2007, 37, 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, 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, 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, 3825-3830; DOI:10.1055/s-2006-950296.
R. H. Manske: The Chemistry of Quinolines., in: Chem. Rev. 1942, 30, 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, 141—161; DOI:10.1002/chin.200516245.
R. H. Reitsema: The Chemistry of 4-Hydroxyquinolines., in: Chem. Rev. 1948, 43, 43-68; DOI:10.1021/cr60134a002.
F. W. Bergstrom, Heterocyclic Nitrogen Compounds. Part IIA. Hexacyclic Compounds: Pyridine, Quinoline, and Isoquinoline., in: Chem. Rev. 1944, 35, 77-277; DOI:10.1021/cr60111a001.
R. Camps: Synthese von alpha- und gamma-Oxychinolinen, in: Chem. Ber. 1899, 22, 3228; DOI:10.1002/cber.18990320389.
L. Knorr: Synthetische Versuche mit dem Acetessigester, in: Liebigs Ann. 1886, 236, 69-115; DOI:10.1002/jlac.18862360105.
Synthetische Versuche mit dem Acetessigester Justus Liebig's Annalen der Chemie Volume 236, Issue 1-2, Date: 1886, Pages: 69-115 Ludwig Knorr 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, 2890—2895; DOI:10.1021/ja01265a088.
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, 526—533; DOI:10.1039/JR9600000526.
J. E. Davies, A. D. Bond: Quinoline, in: Acta Cryst. 2001, E57, S. o947-o949; DOI:10.1107/S1600536801014891.
O. Eckstein: Ueber Chinolin-chlorhydrat und die Einwirkung von Säurechloriden auf Chinolin, in: Chem. Ber. 1906, 39, 2135—2138; DOI:10.1002/cber.190603902173.
G. E. McCasland: The Preparation of 8-Qinolinesulfonic acid, in: J. Org. Chem. 1946, 11, 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, 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, 409—410; DOI:10.1002/jhet.5570100326.
H. van der Plas: Oxidative Amino-Dehydrogenation of Azines, in: Adv. Heterocycl. Chem. 2004, 86, 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, 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, 741—750; DOI:10.1021/jo01176a015.
J. Meisenheimer: Über Pyridin-, Chinolin— und Isochinolin-N-oxyd., in: Ber. Dtsch. Chem. Ges. 1926, 59, 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, 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, 808—811; DOI:10.1021/jo01062a039.
C. O'Murchu: Ozonolysis of Quinolines: A Versatile Synthesis of Polyfunctional Pyridines, in: Synthesis 1989, 11, 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, 1566—1571; DOI:10.1021/jm00127a027.
B. C. Ranua, U. Janaa, A. Sarkara: Regioselective Reduction of Quinolines and Related Systems to 1,2,3,4-Tetrahydro Derivatives with Zinc Borohydride, in: Synth. Commun. 1998, 28, 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-]isoquinolines, in: J. Chem. Soc., Perkin Trans. 1 1995, 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, 3249-3257; DOI:10.1039/JR9600003249.

merck.de

assets.chemportals.merck.de

Технічний лист Хінолін отримано з Merck, 5. September 2010.

nii.ac.jp

ci.nii.ac.jp

A. Nose, T. Kudo: Reduction of Heterocyclic Compounds. II. Reduction of Heterocyclic Compounds with Sodium Borohydride-Transition Metal Salt Systems, in: Chem. Pharm. Bull.(інші мови) 1984, 32, 2421—2425; Abstract [Архівовано 16 серпня 2011 у Wayback Machine.].

orgsynth.org

Organic Syntheses, Coll. Vol. 3, p.272 (1955); Vol. 28, p.38 (1948). Link [Архівовано 8 лютого 2012 у Wayback Machine.]

web.archive.org

Organic Syntheses, Coll. Vol. 3, p.272 (1955); Vol. 28, p.38 (1948). Link [Архівовано 8 лютого 2012 у Wayback Machine.]
A. Nose, T. Kudo: Reduction of Heterocyclic Compounds. II. Reduction of Heterocyclic Compounds with Sodium Borohydride-Transition Metal Salt Systems, in: Chem. Pharm. Bull.(інші мови) 1984, 32, 2421—2425; Abstract [Архівовано 16 серпня 2011 у Wayback Machine.].

wikidata.org

G. Queguiner, P. Pastour: Synthèse dans la série de la pyridine — I — Les diformylpyridines, in: Bull. Soc. Chim. Fr.(інші мови) 1968, 10, 4117-4121.
A. Nose, T. Kudo: Reduction of Heterocyclic Compounds. II. Reduction of Heterocyclic Compounds with Sodium Borohydride-Transition Metal Salt Systems, in: Chem. Pharm. Bull.(інші мови) 1984, 32, 2421—2425; Abstract [Архівовано 16 серпня 2011 у Wayback Machine.].