Collect. Czech. Chem. Commun. 1996, 61, S16-S19
https://doi.org/10.1135/cccc1996s016

Synthesis, conformation and biological properties of 2',3'-dideoxy-3'-fluoro-5-chloro-4-thiouridine, potential anti-HIV agent

Nicolai E. Poopeiko, Alicja K. Drabikowska, Jaroslav Poznanski, David Shugar and Tadeusz Kulikowski

Individual author index pages


Other CCCC articles of these authors

  • Krzysztof Felczak, Agnieszka Miazga and Tadeusz Kulikowski
    Synthesis of novel acyclo 6-phenylselenenyluracils – potential selective anti-HIV agents
    Symposium Series 1999, Vol. 2, pp. 245–247 [Abstract]
    Published online 2016-05-08 23:31:18
  • Grzegorz Mędza, Jacek Wierzchowski and David Shugar
    Fluorescent analogues of caffeine, theophylline, and other methyl-xanthines
    Symposium Series 2008, Vol. 10, pp. 478–479 [Abstract]
    Published online 2015-10-30 18:45:51
  • Jacek Wierzchowski, Grzegorz Mędza and David Shugar
    Excited-state proton transfer in the fluorescent purine analogue – 8-azaisoguanine
    Symposium Series 2008, Vol. 10, pp. 476–477 [Abstract]
    Published online 2015-10-30 18:45:46
  • Tadeusz Kulikowski, Jaroslaw Poznanski, Jan Balzarini, Arthur Van Aerschot and Erik De Clercq
    Synthesis, conformation and anti-HIV activity of 3'-substituted 2',3'-dideoxy-5-hydroxymethyluridines
    1993, Vol. 58, Special Issue, pp. S44–S46 [Abstract]
  • Jacek Wierzchowski and David Shugar
    Amino-imino tautomerism of N(6)-methylformycin, a potent inhibitor of E. coli, but not mammalian, purine nucleoside phosphorylase
    1993, Vol. 58, Special Issue, pp. S14–S17 [Abstract]
  • Janusz Stępiński, Lidia Grabowska, Edward Darżynkiewicz, Andrzej Temeriusz, Ryszard Stolarski, Stanley M. Tahara, David Shugar, Pia Järvinen and Harri Lönnberg
    Synthesis, conformation and hydrolytic stability of modified mRNA 5'-cap structures: P1,P3-dinucleoside triphosphates derived from guanosine and acyclic analogues of 7-methyl-, N2,7-dimethyl- and N2,N2,7-trimethylguanosines
    1990, Vol. 55, Special Issue, pp. S117–S120 [Abstract]