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A Modular Approach to Aryl-C-ribonucleosides via the Allylic Substitution and Ring-Closing Metathesis Sequence. A Stereocontrolled Synthesis of All Four alpha-/beta- and D-/L-C-Nucleoside Stereoisomers

  1. 1.
    SYSNO0368189
    TitleA Modular Approach to Aryl-C-ribonucleosides via the Allylic Substitution and Ring-Closing Metathesis Sequence. A Stereocontrolled Synthesis of All Four alpha-/beta- and D-/L-C-Nucleoside Stereoisomers
    Author(s) Štambaský, J. (GB)
    Kapras, V. (GB)
    Štefko, Martin (UOCHB-X) [320/32]
    Kysilka, O. (CZ)
    Hocek, Michal (UOCHB-X) [320/32] RID, ORCID
    Malkov, A. V. (GB)
    Kočovský, P. (GB)
    Source Title Journal of Organic Chemistry. Roč. 76, č. 19 (2011), s. 7781-7803. - : American Chemical Society
    Document TypeČlánek v odborném periodiku
    Grant LC512 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    IAA400550902 GA AV ČR - Academy of Sciences of the Czech Republic (AV ČR)
    CEZAV0Z40550506 - UOCHB-X (2005-2011)
    Languageeng
    CountryUS
    Keywords C-nucleosides * allylic substitution * metathesis * dihydroxylation
    Permanent Linkhttp://hdl.handle.net/11104/0202600
     
Number of the records: 1  

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