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New fluorinated nucleoside analogues with 2-butenolide rings prepared by nucleophilic vinylic fluorine displacement in 4,4-dialkyl-2,3-difluorobut-2-en-4-olides..

  1. 1.
    SYSNO ASEP0194330
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JOstatní články
    TitleNew fluorinated nucleoside analogues with 2-butenolide rings prepared by nucleophilic vinylic fluorine displacement in 4,4-dialkyl-2,3-difluorobut-2-en-4-olides..
    Author(s) Paleta, O. (CZ)
    Duda, Z. (CZ)
    Holý, Antonín (UOCHB-X)
    Source TitleMendeleev Communications. - : Elsevier - ISSN 0959-9436
    - (2001), s. 17-19
    Number of pages3 s.
    Languageeng - English
    CountryRU - Russian Federation
    Keywordsnucleoside analogues
    Subject RIVCC - Organic Chemistry
    R&D ProjectsGA203/96/1057 GA ČR - Czech Science Foundation (CSF)
    LB98233 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    CEZAV0Z4055905 - UOCHB-X
    AnnotationSodium salts of purine and pyrimidine bases with 4,4-dialkyl-2,3-difluorobut-2-en-4-olides gave 3-substituted butenolides as nucleoside analogues.
    WorkplaceInstitute of Organic Chemistry and Biochemistry
    Contactasep@uochb.cas.cz ; Kateřina Šperková, Tel.: 232 002 584 ; Jana Procházková, Tel.: 220 183 418
    Year of Publishing2002

Number of the records: 1  

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