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Synthesis of purine nucleoside analogues derived from carbocyclic 5-C-(hydroxymethyl)hexopyranoses

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    0100872 - UOCHB-X 20043060 RIV CZ eng J - Journal Article
    Hřebabecký, Hubert - Masojídková, Milena - Holý, Antonín
    Synthesis of purine nucleoside analogues derived from carbocyclic 5-C-(hydroxymethyl)hexopyranoses.
    [Synthesa analog purinových nukleosidů odvozených od karbocyklických 5-C-(hydroxymethyl)hexopyranos.]
    Collection of Czechoslovak Chemical Communications. Roč. 69, č. 2 (2004), s. 435-452. ISSN 0010-0765
    R&D Projects: GA ČR GA203/02/0035
    Institutional research plan: CEZ:AV0Z4055905
    Keywords : nucleosides * purines * adenine
    Subject RIV: CC - Organic Chemistry
    Impact factor: 1.062, year: 2004

    New nucleoside analogues of adenine, 6-(cyclopropylamino)purine, and guanine were prepared from amino derivatives of 5a-carba-5-C-(hydroxymethyl)-alpha-D-idopyranose and 5a-carba-5-C-(hydroxymethyl)-beta-D-gulopyranose

    Nová nukleosidová analoga adeninu, 6-(cyklopropylamino)purinu a guaninu byla připravena z aminoderivátů 5a-karba-5-C-(hydroxymethyl)-alfa-D-idopyranosy a karba-5-C-(hydroxymethyl)-beta-D-gulopyranosy
    Permanent Link: http://hdl.handle.net/11104/0008356

     
     

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