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One-pot synthesis of 4-substituted 2-fluoroalkyloxazoles from NH-1,2,3-triazoles and fluoroalkylated acid anhydrides

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F22%3A00559497" target="_blank" >RIV/61388963:_____/22:00559497 - isvavai.cz</a>

  • Result on the web

    <a href="https://doi.org/10.1039/D2NJ02461F" target="_blank" >https://doi.org/10.1039/D2NJ02461F</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1039/d2nj02461f" target="_blank" >10.1039/d2nj02461f</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    One-pot synthesis of 4-substituted 2-fluoroalkyloxazoles from NH-1,2,3-triazoles and fluoroalkylated acid anhydrides

  • Original language description

    An efficient one-pot method for the synthesis of 2-fluoroalkyloxazoles from 4-substituted NH-1,2,3-triazoles, fluorinated anhydrides and triethylamine was developed. Structurally diverse fluoroalkylated oxazoles (RF = CF3, C2F5, CF2Cl, CF2H) were prepared in high yields from readily available starting reagents in mild conditions. An alternative direct method for fluoroalkylated oxazole synthesis from electron-rich NH-triazoles using acetonitrile as the solvent was described.

  • 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/LTAUSA18037" target="_blank" >LTAUSA18037: Synthesis and reactivity of N-fluoroalkylated compounds</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

    New Journal of Chemistry

  • ISSN

    1144-0546

  • e-ISSN

    1369-9261

  • Volume of the periodical

    46

  • Issue of the periodical within the volume

    30

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    6

  • Pages from-to

    14318-14323

  • UT code for WoS article

    000826637300001

  • EID of the result in the Scopus database

    2-s2.0-85134986765