Number of the records: 1  

Synthesis of N4-amino and N4-hydroxy derivatives of 5-azacytidine. A facile rearrangement of the N4-amino derivative to 5-(3-beta-D-ribofuranosylureido)-1H-1,2,4-triazole

  1. 1.
    0100877 - UOCHB-X 20043065 RIV CZ eng J - Journal Article
    Pískala, Alois - Hanna, N. B. - Masojídková, Milena - Fiedler, Pavel - Votruba, Ivan
    Synthesis of N4-amino and N4-hydroxy derivatives of 5-azacytidine. A facile rearrangement of the N4-amino derivative to 5-(3-beta-D-ribofuranosylureido)-1H-1,2,4-triazole.
    [Syntéza N4-amino a N4-hydroxyderivátů 5-azacytidinu. Snadný přesmyk N4-aminoderivátu na 5-(3-beta-D-ribofuranosylureido)-1H-1,2,4-triazol.]
    Collection of Czechoslovak Chemical Communications. Roč. 69, č. 4 (2004), s. 905-917. ISSN 0010-0765
    Institutional research plan: CEZ:AV0Z4055905
    Keywords : 1,3,5-triazines * nucleosides * antibacterial activity
    Subject RIV: CC - Organic Chemistry
    Impact factor: 1.062, year: 2004

    N4-Amino and N4-Hydroxy derivatives of the nucleoside antibiotic 5-azacytidine have been prepared. A facile rearrangement of the N4-amino derivative to 5-(3-beta-D-ribofuranosylureido)-1H-1,2,4-triazole and its mechanism was described

    Byly připaveny N4-amino- a N4-hydroxyderiváty nukleosidového antibiotika 5-azacytidinu. Byl popsán snadný přesmyk tohoto N4-aminoderivátu na 5-(3-beta-D-ribofuranosylureido)-1H-1,2,4-triazol a jeho mechanismus
    Permanent Link: http://hdl.handle.net/11104/0008361


     
     

Number of the records: 1  

  This site uses cookies to make them easier to browse. Learn more about how we use cookies.