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Chiral separation and spectroscopic characterization of mefloquine analogues

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22310%2F25%3A43933880" target="_blank" >RIV/60461373:22310/25:43933880 - isvavai.cz</a>

  • Alternative codes found

    RIV/60461373:22340/25:43933880

  • Result on the web

    <a href="https://doi.org/10.1016/j.saa.2024.124940" target="_blank" >https://doi.org/10.1016/j.saa.2024.124940</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.saa.2024.124940" target="_blank" >10.1016/j.saa.2024.124940</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Chiral separation and spectroscopic characterization of mefloquine analogues

  • Original language description

    Mefloquine, a widely used antimalarial agent, has spurred ongoing research into the development of derivatives with enhanced efficacy and reduced side effects. In this investigation, we synthesized two compounds containing N-allyl or N-tert-butylacetamid groups. A chiral liquid chromatography with polysaccharide chiral stationary phase was utilized to separate the enantiomers of both derivatives. We employed spectroscopic chiroptical and non-polarizable methods such as electronic and vibrational circular dichroism, infrared absorption and ultraviolet spectroscopies. Combined with density functional theory calculations, the stable conformers were found in solution and their spectra were subsequently simulated. We elucidated the three-dimensional structure of the enantiomerically pure compounds and assigned the absolute configuration of all prepared derivatives using both experimental and simulated spectra.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    21100 - Other engineering and technologies

Result continuities

  • Project

    <a href="/en/project/GC21-31139J" target="_blank" >GC21-31139J: Novel chiral ion-exchangers for chromatographic enantioseparations</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2025

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY

  • ISSN

    1386-1425

  • e-ISSN

    1873-3557

  • Volume of the periodical

    324

  • Issue of the periodical within the volume

    5 January 2025

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    10

  • Pages from-to

    nestránkováno

  • UT code for WoS article

    001300347000001

  • EID of the result in the Scopus database

    2-s2.0-85201634286