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Determination of enantiopurity of new types of acyclic nucleoside phosphonates by capillary electrophoresis with cyclodextrins-based chiral selectors

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    SYSNO ASEP0430071
    Document TypeC - Proceedings Paper (int. conf.)
    R&D Document TypeThe record was not marked in the RIV
    TitleDetermination of enantiopurity of new types of acyclic nucleoside phosphonates by capillary electrophoresis with cyclodextrins-based chiral selectors
    Author(s) Šolínová, Veronika (UOCHB-X) RID, ORCID
    Kaiser, Martin Maxmilian (UOCHB-X) RID, ORCID
    Lukáč, Miloš (UOCHB-X)
    Janeba, Zlatko (UOCHB-X) RID, ORCID
    Kašička, Václav (UOCHB-X) RID, ORCID
    Number of authors5
    Source TitleActa Universitatis Palackianae Olomucensis. Facultas Rerum Naturalium. Chemica 51S. - Olomouc : Palacký University, 2014 / Maier V. ; Ševčík J. - ISSN 0232-0061 - ISBN 978-80-244-3950-1
    Pagess. 207-209
    Number of pages3 s.
    Publication formPrint - P
    ActionAdvances in Chromatography and Electrophoresis & Chiranal 2014
    Event date10.02.2014-14.02.2014
    VEvent locationOlomouc
    CountryCZ - Czech Republic
    Event typeEUR
    Languageeng - English
    CountryCZ - Czech Republic
    Keywordsacyclic nucleoside phosphonates ; capillary electrophoresis ; enantiopurity analysis
    Subject RIVCB - Analytical Chemistry, Separation
    R&D ProjectsGAP206/12/0453 GA ČR - Czech Science Foundation (CSF)
    GA13-17224S GA ČR - Czech Science Foundation (CSF)
    VG20102015046 GA MV - Ministry of Interior (MV)
    Institutional supportUOCHB-X - RVO:61388963
    AnnotationCapillary electrophoresis with neutral and cationic cyclodextrins as chiral selectors was applied for determination of enantiopurity analysis of new types of six acyclic nucleoside phosphonates, nucleotide analogues bearing ((3-hydroxypropan-2-yl)-1H-1,2,3-triazol-4-yl)phosphonic acid, 2-((diisopropoxyphosphonyl)methoxy)propanoic acid or 2 (phosphonomethoxy)propanoic acid moieties attached to adenine, guanine, 2,6-diaminopurine, uracil and 5-bromouracil nucleobases. All these compounds were found to be synthesized in pure enantiomeric forms. Employing the UV-absorption detection at 206 nm, their detection limits were in the low micromolar level.
    WorkplaceInstitute of Organic Chemistry and Biochemistry
    Contactasep@uochb.cas.cz ; Kateřina Šperková, Tel.: 232 002 584 ; Jana Procházková, Tel.: 220 183 418
    Year of Publishing2015
Number of the records: 1  

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