Хінолін (Ukrainian Wikipedia)

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

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  • 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.
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  • 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.
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  • 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.
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  • 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.
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  • 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.
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  • 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 (±)-[4aα,4bβ,10bβ,12aα]-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.

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

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