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A new route alpha-alkyl-alpha-fluoromethylenebisphosphonates

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    SYSNO ASEP0360949
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleA new route alpha-alkyl-alpha-fluoromethylenebisphosphonates
    Author(s) Beier, Petr (UOCHB-X) RID, ORCID
    Opekar, Stanislav (UOCHB-X)
    Zibinsky, M. (US)
    Bychinskaya, I. (US)
    Prakash, G. K. S. (US)
    Number of authors5
    Source TitleOrganic & Biomolecular Chemistry. - : Royal Society of Chemistry - ISSN 1477-0520
    Roč. 9, č. 11 (2011), s. 4035-4038
    Number of pages4 s.
    Languageeng - English
    CountryGB - United Kingdom
    Keywordsfluorine ; phosphonate ; alkylation
    Subject RIVCC - Organic Chemistry
    R&D ProjectsGP203/08/P310 GA ČR - Czech Science Foundation (CSF)
    CEZAV0Z40550506 - UOCHB-X (2005-2011)
    UT WOS000290735300008
    DOI10.1039/c1ob05095h
    AnnotationA new route to alpha-alkyl-alpha-fluoromethylenebisphosphonates (2) has been developed starting from commercially available tetraethyl fluoromethylenebisphosphonate (1), and alkyl halides using either cesium carbonate in DMF or sodium dimsyl. De-esterification of 2 provided biologically important alpha-alkyl-alpha-fluoromethylenebisphosphonic acid (3), while alkoxide–induced carbon–phosphorus bond cleavage of 2 gave alfa-fluorophosphonates (4), which are useful synthons in organic synthesis.
    WorkplaceInstitute of Organic Chemistry and Biochemistry
    Contactasep@uochb.cas.cz ; Kateřina Šperková, Tel.: 232 002 584 ; Jana Procházková, Tel.: 220 183 418
    Year of Publishing2012
Number of the records: 1  

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