Інсерція (Ukrainian Wikipedia)

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

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  • Arndt, F.; Eistert, B. (1935). Ein Verfahren zur Überführung von Carbonsäuren in ihre höheren Homologen bzw. deren Derivate. Ber. Dtsch. Chem. Ges. (German) . 68 (1): 200—208. doi:10.1002/cber.19350680142.
  • Ye, T.; McKervey, M. A. (1994). Organic Synthesis with α-Diazo Carbonyl Compounds. Chem. Rev. 94 (4): 1091—1160. doi:10.1021/cr00028a010.
  • Huggett, C.; Arnold, R. T.; Taylor, T. I. (1942). The Mechanism of the Arndt-Eistert Reaction. J. Am. Chem. Soc. 64 (12): 3043. doi:10.1021/ja01264a505.
  • Meier, H.; Zeller, K.-P. (1975). The Wolff Rearrangement of α-Diazo Carbonyl Compounds. Angew. Chem. Int. Ed. 14 (1): 32—43. doi:10.1002/anie.197500321.
  • Kirmse, W. (2002). 100 Years of the Wolff Rearrangement. Eur. J. Org. Chem. 2002 (14): 2193—2256. doi:10.1002/1099-0690(200207)2002:14<2193::AID-EJOC2193>3.0.CO;2-D.
  • Clibbens, D. A.; Nierenstein, M. (1915). The Action of Diazomethane on some Aromatic Acyl Chlorides. J. Chem. Soc., Trans. 107: 1491—1494. doi:10.1039/CT9150701491.
  • Nierenstein, M.; Wang, D. G.; Warr, J. C. (1924). The Action of Diazomethane on some Aromatic Acyl Chlorides II. Synthesis of Fisetol. J. Am. Chem. Soc. 46 (11): 2551—2555. doi:10.1021/ja01676a028.
  • Lewis, H. H.; Nierenstein, M.; Rich, E. M. (1925). The Action of Diazomethane on some Aromatic Acyl Chlorides III. The Mechanism of the Reaction. J. Am. Chem. Soc. 47 (6): 1728—1732. doi:10.1021/ja01683a036.
  • Reed, D. D.; Bergmeier, S. C. (2007). A Facile Synthesis of a Polyhydroxylated 2-Azabicyclo[3.2.1]octane. J. Org. Chem. 72 (3): 1024—1026. doi:10.1021/jo0619231. PMID 17253828.
  • Beckmann, E. (1886). Zur Kenntniss der Isonitrosoverbindungen. Ber. Dtsch. Chem. Ges. (German) . 19: 988—993. doi:10.1002/cber.188601901222.
  • Gawley, R. E. (1988). The Beckmann Reactions: Rearrangement, Elimination-Additions, Fragmentations, and Rearrangement-Cyclizations. Org. React. 35: 14—24. doi:10.1002/0471264180.or035.01. ISBN 0471264180.
  • Ritz, J.; Fuchs, H.; Kieczka, H.; Moran, W. C. (2000). Caprolactam. Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a05_031. ISBN 3527306730.
  • Blakemore, P. R.; Burge, M. S. (2007). Iterative Stereospecific Reagent-Controlled Homologation of Pinacol Boronates by Enantioenriched-Chloroalkyllithium Reagents. J. Am. Chem. Soc. 129 (11): 3068—3069. doi:10.1021/ja068808s. PMID 17326640.
  • Jones, J. H. (2000). The Cativa Process for the Manufacture of Acetic Acid (PDF). Platinum Metals Rev. 44 (3): 94—105. doi:10.1595/003214000X44394105. Архів оригіналу (PDF) за 24 вересня 2015. Процитовано 22 грудня 2010.
  • Sunley, G. J.; Watson, D. J. (2000). High Productivity Methanol Carbonylation Catalysis using Iridium - The Cativa Process for the Manufacture of Acetic Acid. Catalysis Today. 58 (4): 293—307. doi:10.1016/S0920-5861(00)00263-7.

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