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Synthesis of sulfur karrikin bioisosteres as potential neuroprotectives

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F22%3A00558020" target="_blank" >RIV/61388963:_____/22:00558020 - isvavai.cz</a>

  • Result on the web

    <a href="https://doi.org/10.3762/bjoc.18.57" target="_blank" >https://doi.org/10.3762/bjoc.18.57</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.3762/bjoc.18.57" target="_blank" >10.3762/bjoc.18.57</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Synthesis of sulfur karrikin bioisosteres as potential neuroprotectives

  • Original language description

    The only known sulfur-containing karrikin, 3-methyl-2H-thiopyrano[3,4-b]furan-2-one, has been recently identified as an extremely efficient neuroprotective butenolide. Herein, we report the targeted synthesis of this compound as well as new synthetic protocols toward a class of compounds derived from 2H-furo[2,3-c]pyran-2-ones (karrikins) via bioisosteric exchange of oxygen with sulfur. In particular, we present synthetic procedures toward bioisosteres of karrikins with one or two sulfur heteroatoms incorporated into the core backbone together with evaluation of their biological activity in inhibition of acetylcholinesterase.

  • 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

    10401 - Organic chemistry

Result continuities

  • Project

    <a href="/en/project/GA20-11571S" target="_blank" >GA20-11571S: Butenolides with neuroprotective effect from plant-derived smoke and their synthetic derivatives</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2022

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Beilstein Journal of Organic Chemistry

  • ISSN

    1860-5397

  • e-ISSN

    1860-5397

  • Volume of the periodical

    18

  • Issue of the periodical within the volume

    May

  • Country of publishing house

    DE - GERMANY

  • Number of pages

    6

  • Pages from-to

    549-554

  • UT code for WoS article

    000799976100001

  • EID of the result in the Scopus database

    2-s2.0-85132237725