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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

Open Access
|May 2013

References

  1. Bella M, Schultz M, Milata V (2012) Arkivoc IV: 242-251.10.3998/ark.5550190.0013.418
  2. Claisen L (1893) Chem. Ber. 26: 2729-2735.10.1002/cber.18930260375
  3. Couchouron B, Le Saint J, Courtot P (1983) Bull. Soc. Chim. Fr. II: 66-71.
  4. Darque A, Dumetre A, Hutter S, Azas N, Casano G, Robin M, Pannecouque Ch (2009) Bioorg. Med. Chem. Lett. 19: 5962-5964.
  5. Deshmukh ARAS, Panse DG, Bhawal BM (1999) Synth. Commun. 29: 1801-1810.
  6. Ewing DF (1979) Org. Magn. Reson. 12: 499-524.
  7. Fodor G, Wein J, Schonberg A, Duffin GF, Kendall JD, Seetharamiah A (1948) J. Chem. Soc. 890-895.10.1039/JR9480000890
  8. Goljer I, Milata V, Ilavsky D (1989) Magn. Reson. Chem. 27: 138-144.
  9. Hansen PE, Bolvig S, Duus F, Petrova MV, Kawecki R, Krajewski R, Kozerski L (1995) Magn. Reson. Chem. 33: 621-631.
  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.
  11. Huppatz JL, Phillips JN, Rattigan BM (1981) Agricult. Biol. Chem., 45: 2769-2774.
  12. Kim KW, Lee HJ, Jo JI, Kwon, TW (2010) Bull. Korean Chem. Soc. 31: 1155-1158.
  13. Lager E, Andersson P, Nilsson J, Pettersson I, Nielsen EO, Nielsen M, Sterner O, Liljefors T (2006) J. Med. Chem. 49: 2526-2533.
  14. Lopez R, Marisa J, Moyano EL, Yranzo GI (2010) Tetrahedron Lett. 51: 478-481.
  15. Loupy A, Song SJ, Cho SJ, Park DK, Kwon TW (2005) Synth. Commun. 35: 79-88.
  16. Mao D, Xu J, Hu X, Dong J, Zhang G, Gong G (2009) Chem. Biodiv. 6: 1727-1736.
  17. da Matta AD, Bernardino AMR, Romeiro GA, de Oliveira MRP, Souza MCBV, deFerreira VF (1996) Nucleosides & Nucleotides 15: 889-898.10.1080/07328319608002135
  18. Milata V, Ilavsky D (1987) Coll. Czechoslov. Chem. Commun. 52: 2918-2925.
  19. Mohri K, Kanie A, Horiguchi Y, Isobe K (1999) Heterocycles 51: 2377-2384.10.3987/COM-99-8629
  20. Mukhopadhyaya JK, Sklenak S, Rappoport Z (2000) J. Org. Chem. 65: 6856-6867.
  21. Nasakin O, Lyshchikov AN, Lukin PM, Tafeenko VA, Bulai AKh, Medvedev SV (1992) Chem. Het. Comp. 28: 1124-1129.
  22. Rao V, Balakrishnan M, Venkatasubramanian N (1974) Indian J. Chem. 13: 1090-1091.
  23. Rappoport Z, Topol A (1972) J. Chem. Soc. Perkin Trans. 2: 1823-1831.10.1039/P29720001823
  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.
  25. Santilli AA (1964) J. Med. Chem. 7: 68-72.
  26. Snyder J, Jones RE (1946) J. Am. Chem. Soc. 68: 1253-1255.
  27. Wolfbeis OS (1977) Synth. 723-725.
  28. Wolfbeis OS, Junek HZ (1979) Naturforsch. [B] 34: 283-286.
  29. Zewge D, Chen Ch-Y, Deer C, Dormer PG, Hughes DL (2007) J. Org. Chem. 72: 4276-4279.
DOI: https://doi.org/10.2478/acs-2013-0013 | Journal eISSN: 1339-3065 | Journal ISSN: 1337-978X
Language: English
Page range: 73 - 81
Published on: May 22, 2013
In partnership with: Paradigm Publishing Services
Publication frequency: 1 issue per year
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© 2013 Denisa Tarabová, Viktor Milata, Jiří Hanusek, published by Slovak University of Technology in Bratislava
This work is licensed under the Creative Commons License.