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Preparation and NMR properties of derivatives of arylamino-methylidene malonic acid and pentane-2,4-dione Cover

Preparation and NMR properties of derivatives of arylamino-methylidene malonic acid and pentane-2,4-dione

Acta Chimica Slovaca
Volume 6 (2013): Issue 1 (April 2013)
By: ,   and    
Open Access
|May 2013
References

References

  1. Bella M, Schultz M, Milata V (2012) Arkivoc IV: 242-251.
    Open DOISearch in Google Scholar
  2. Claisen L (1893) Chem. Ber. 26: 2729-2735.
    Open DOISearch in Google Scholar
  3. Couchouron B, Le Saint J, Courtot P (1983) Bull. Soc. Chim. Fr. II: 66-71.
    Search in Google Scholar
  4. Darque A, Dumetre A, Hutter S, Azas N, Casano G, Robin M, Pannecouque Ch (2009) Bioorg. Med. Chem. Lett. 19: 5962-5964.
    Search in Google Scholar
  5. Deshmukh ARAS, Panse DG, Bhawal BM (1999) Synth. Commun. 29: 1801-1810.
    Search in Google Scholar
  6. Ewing DF (1979) Org. Magn. Reson. 12: 499-524.
    Search in Google Scholar
  7. Fodor G, Wein J, Schonberg A, Duffin GF, Kendall JD, Seetharamiah A (1948) J. Chem. Soc. 890-895.
    Open DOISearch in Google Scholar
  8. Goljer I, Milata V, Ilavsky D (1989) Magn. Reson. Chem. 27: 138-144.
    Search in Google Scholar
  9. Hansen PE, Bolvig S, Duus F, Petrova MV, Kawecki R, Krajewski R, Kozerski L (1995) Magn. Reson. Chem. 33: 621-631.
    Search in Google Scholar
  10. Hermecz I, Kereszturi G, Vasvari-Debreczy L (1992) in Advances in Heterocyclic Chemistry, Vol. 54: Aminomethylenemalonates and Their Use in Heterocyclic Synthesis, ed. A.R. Katritzky, Academic Press, San Diego, 452 p.
    Search in Google Scholar
  11. Huppatz JL, Phillips JN, Rattigan BM (1981) Agricult. Biol. Chem., 45: 2769-2774.
    Search in Google Scholar
  12. Kim KW, Lee HJ, Jo JI, Kwon, TW (2010) Bull. Korean Chem. Soc. 31: 1155-1158.
    Search in Google Scholar
  13. Lager E, Andersson P, Nilsson J, Pettersson I, Nielsen EO, Nielsen M, Sterner O, Liljefors T (2006) J. Med. Chem. 49: 2526-2533.
    Search in Google Scholar
  14. Lopez R, Marisa J, Moyano EL, Yranzo GI (2010) Tetrahedron Lett. 51: 478-481.
    Search in Google Scholar
  15. Loupy A, Song SJ, Cho SJ, Park DK, Kwon TW (2005) Synth. Commun. 35: 79-88.
    Search in Google Scholar
  16. Mao D, Xu J, Hu X, Dong J, Zhang G, Gong G (2009) Chem. Biodiv. 6: 1727-1736.
    Search in Google Scholar
  17. da Matta AD, Bernardino AMR, Romeiro GA, de Oliveira MRP, Souza MCBV, deFerreira VF (1996) Nucleosides & Nucleotides 15: 889-898.
    Open DOISearch in Google Scholar
  18. Milata V, Ilavsky D (1987) Coll. Czechoslov. Chem. Commun. 52: 2918-2925.
    Search in Google Scholar
  19. Mohri K, Kanie A, Horiguchi Y, Isobe K (1999) Heterocycles 51: 2377-2384.
    Open DOISearch in Google Scholar
  20. Mukhopadhyaya JK, Sklenak S, Rappoport Z (2000) J. Org. Chem. 65: 6856-6867.
    Search in Google Scholar
  21. Nasakin O, Lyshchikov AN, Lukin PM, Tafeenko VA, Bulai AKh, Medvedev SV (1992) Chem. Het. Comp. 28: 1124-1129.
    Search in Google Scholar
  22. Rao V, Balakrishnan M, Venkatasubramanian N (1974) Indian J. Chem. 13: 1090-1091.
    Search in Google Scholar
  23. Rappoport Z, Topol A (1972) J. Chem. Soc. Perkin Trans. 2: 1823-1831.
    Open DOISearch in Google Scholar
  24. Saloň J, Milata V, Gatial A, Pronayova N, Leško J, Černuchova P, Rappoport Z, Vo-Thanh G, Loupy A (2005) Eur. J. Org. Chem. 22: 4870-4878.
    Search in Google Scholar
  25. Santilli AA (1964) J. Med. Chem. 7: 68-72.
    Search in Google Scholar
  26. Snyder J, Jones RE (1946) J. Am. Chem. Soc. 68: 1253-1255.
    Search in Google Scholar
  27. Wolfbeis OS (1977) Synth. 723-725.
    Search in Google Scholar
  28. Wolfbeis OS, Junek HZ (1979) Naturforsch. [B] 34: 283-286.
    Search in Google Scholar
  29. Zewge D, Chen Ch-Y, Deer C, Dormer PG, Hughes DL (2007) J. Org. Chem. 72: 4276-4279.
    Search in Google Scholar
DOI: https://doi.org/10.2478/acs-2013-0013 | Journal eISSN: 1339-3065 (formerly 1337-978X) | Journal ISSN: 1337-978X
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Language: English
Page range: 73 - 81
Published on: May 22, 2013
Published by: Slovak University of Technology in Bratislava
In partnership with: Paradigm Publishing Services
Publication frequency: 1 issue per year
Keywords:
NMR spectroscopy,
substituent chemical shifts (SCS),
arylaminomethylidene derivatives,
enamines
Related subjects:
Chemistry,
Chemistry, other

© 2013 Denisa Tarabová, Viktor Milata, Jiří Hanusek, published by Slovak University of Technology in Bratislava
This work is licensed under the Creative Commons License.

Volume 6 (2013): Issue 1 (April 2013)
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