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Tytuł artykułu

Synthesis and structure of Two thiocarboxypyrazolic Acid Derivatives

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Two thiocarboxypyrazolic acid amide derivatives were obtained unintentionally in a reaction of thiosemicarbazone with 2-acetylbutyrolactone, and structures of the final products have been determined by X-ray diffraction. Due to conjugation of the thioamide group with the planar pyrazolic ring, the molecule is flat, except 2-hydroxylethyl chain, accidentally adopting similar conformation in the two studied molecules. Also similar is the packing, despite different hydrogen bonding schemes, resulting from the different number of donoric H atoms and the presence of an additional water molecule in the second compound. The mechanism of the reaction is suggested.
Rocznik
Strony
2013--2022
Opis fizyczny
Bibliogr. 16 poz., rys.
Twórcy
autor
  • Institute of General and Ecological Chemistry, Technical University of Łódź, ul. Żeromskiego 116, 90-924 Łódź, Poland
  • Institute of General and Ecological Chemistry, Technical University of Łódź, ul. Żeromskiego 116, 90-924 Łódź, Poland
  • Section of Inorganic and Analytical Chemistry, Department of Chemistry, University of Ioannina, 45110 Ioannina, Greece
autor
  • Section of Inorganic and Analytical Chemistry, Department of Chemistry, University of Ioannina, 45110 Ioannina, Greece
  • Section of Inorganic and Analytical Chemistry, Department of Chemistry, University of Ioannina, 45110 Ioannina, Greece
Bibliografia
  • 1. Liberta A.E. and West D.X., Biometals, 5, 121 (1992).
  • 2. Kovala-Demertzi D., KourkoumelisN., Demertzis M.A., Miller J.R, Frampton C., Swearingen J.K. an West D.X., Eur. J. Inorg. Chem., 727 (2000).
  • 3. VaradinovaT., Kovala-Demertzi D., Rupelieva M., Demertzis M. and Genova P., Acta Virologica, 45,87(2001).
  • 4. Quiroga A.G., Pérez J.M., López-Solera I., Masaquer J.R, Luque A., Román P., Edwards A., Alonso C and Navarro-Ranninger C., J. Med Chem., 41,1399 (1998).
  • 5. Kovala-Demertzi D., Nath Yadav P., Demertzis M.A. and Coluccia M., J. Inorg. Biochem., 78, 347 (2000).
  • 6. Iakovidou Z., Mioglou E., Mourelatos D., Kotsis A., Demertzis M.A., Papagoergiou A., Nath Yadav P and Kovala-Demertzi D., Anticancer Drugs, 12, 65 (2001).
  • 7. Kovala-Demertzi D., Demertzis M.A., Miller J.R., Frampton C.S., Jasinski J.P. and West D.X., J. Inorg Biochem., 92,137 (2002) (and references therein).
  • 8. Attanasi O.A, De Crescentini L., Filippone P., Foresti E., Galeazzi R, Ghiviriga I. and Katritzky A.R., Tetrahedron, 53, 5617 (1997).
  • 9. Attanasi O.A., Buratti S., Filippone P., Fiorucci C. and Foresti E., Tetrahedron, 52, 1579 (1996).
  • 10. Attanasi O.A., Foresti E., Liao Zhiyuan and Serra-Zanetti F., J. Org. Chem., 60, 149 (1995).
  • 11. Carballo R, Casas J.S., Garcia-Martinez E., Pereiras-Gabian G., Sanchez A., Sordo J. and Vazquez-Lopez E.M., Acta Cryst., E58, o787 (2002).
  • 12. Casas J.S., Castaño M.V., Castellano E.E., Garcia-Tasende M.S., Sanchez A., Sanjuan M.L. and Sordo J., Eur. J. Inorg. Chem., 83 (2000).
  • 13. Allen F.H., Acta Cryst., B58, 380 (2002). Cambridge Structure Database, ver. 5.25 (2003). CSD REFCODES: BESGAH, BIYGUL, CXPAMP, CYMUDOIO, DCPZCOIO, DXABIM01, DXABIM10, HOXLAH, JEWPIK, JEWSOT, JEWSUZ, JEWSUZ01, JEWTAG, JWETEK, MTZTUD10, MXZTCE10, SOXBMB, TMZBCOIO, WAYHEJ, WOYWAI, ZUKSAZ.
  • 14. Sheldríck G.M., SHELXTL/PC, User Manual. Simens Analytical Instrument. An Integrated System for Solving, Refining and Displaying Crystal Structures from Diffraction Data, Siemens Analytical X-Ray Instruments, Inc. Medison, Wisconsin, USA (1990).
  • 15. Sheldrick G.M., SHELXL97. Program for Refinement of Crystal Structures. University of Gottingen, Germany (1997).
  • 16. Etter M.C., MacDonald J.C. and Bernstein J., Acta Cryst., B46, 262 (1990).
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BUJ1-0024-0139
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