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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.
    0194330 - UOCHB-X 20010175 RIV RU eng J - Journal Article
    Paleta, O. - Duda, Z. - Holý, Antonín
    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.
    Mendeleev Communications. - (2001), s. 17-19. ISSN 0959-9436. E-ISSN 1364-551X
    R&D Projects: GA ČR GA203/96/1057; GA MŠMT LB98233
    Institutional research plan: CEZ:AV0Z4055905
    Keywords : nucleoside analogues
    Subject RIV: CC - Organic Chemistry
    Impact factor: 0.711, year: 2001

    Sodium salts of purine and pyrimidine bases with 4,4-dialkyl-2,3-difluorobut-2-en-4-olides gave 3-substituted butenolides as nucleoside analogues.
    Permanent Link: http://hdl.handle.net/11104/0090008

     
     

Number of the records: 1  

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