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Synthesis of benzamide C-ribonucleosides by Pd-catalyzed aminocarbonylations

  1. 1.
    SYSNO ASEP0326283
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleSynthesis of benzamide C-ribonucleosides by Pd-catalyzed aminocarbonylations
    Author(s) Štefko, Martin (UOCHB-X)
    Pohl, Radek (UOCHB-X) RID, ORCID
    Hocek, Michal (UOCHB-X) RID, ORCID
    Number of authors3
    Source TitleTetrahedron. - : Elsevier - ISSN 0040-4020
    Roč. 65, č. 23 (2009), s. 4471-4483
    Number of pages13 s.
    Languageeng - English
    CountryGB - United Kingdom
    KeywordsC-nucleosides ; carbonylations ; carboxamides
    Subject RIVCC - Organic Chemistry
    R&D ProjectsLC512 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)
    UT WOS000266431600003
    DOI10.1016/j.tet.2009.04.006
    AnnotationA novel modular, efficient and practical methodology for preparation of p- and m-substituted benzamide-C-ribonucleosides was developed based on Pd-catalyzed aminocarbonylations of bromobenzene-C-nucleosides.
    WorkplaceInstitute of Organic Chemistry and Biochemistry
    Contactasep@uochb.cas.cz ; Kateřina Šperková, Tel.: 232 002 584 ; Viktorie Chládková, Tel.: 232 002 434
    Year of Publishing2010
Number of the records: 1  

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