888026-87-7Relevant academic research and scientific papers
Antitumour tiazofurin analogues embedded with an amide moiety at the C-2′ position
Popsavin, Mirjana,Svircev, Milos,Torovic, Ljilja,Bogdanovic, Gordana,Kojic, Vesna,Jakimov, Dimitar,Spaic, Sasa,Aleksic, Lidija,Popsavin, Velimir
supporting information; experimental part, p. 6847 - 6858 (2011/10/02)
Synthesis of four new tiazofurin analogues has been accomplished starting from d-glucose. The key step of the synthesis was the three-step cascade that enabled an efficient hydrogen sulfide mediated one-pot conversion of 2-azido-3-O-acyl-ribofuranosyl cya
Synthesis and antiproliferative activity of two new tiazofurin analogues with 2′-amido functionalities
Popsavin, Mirjana,Torovic, Ljilja,Svircev, Milos,Kojic, Vesna,Bogdanovic, Gordana,Popsavin, Velimir
, p. 2773 - 2776 (2007/10/03)
Two novel tiazofurin analogues 2 and 3 were synthesized starting from d-glucose. The key step of the synthesis was the efficient one-step hydrogen sulfide-mediated conversion of 2-azido-3-O-acyl-ribofuranosyl cyanides to the corresponding 2-amido thiocarb
