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Copper-Catalyzed Selective N-Arylation of Oxadiazolones by Diaryliodonium Salts

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22310%2F21%3A43934059" target="_blank" >RIV/60461373:22310/21:43934059 - isvavai.cz</a>

  • Result on the web

    <a href="https://doi.org/10.1002/adsc.202100426" target="_blank" >https://doi.org/10.1002/adsc.202100426</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1002/adsc.202100426" target="_blank" >10.1002/adsc.202100426</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Copper-Catalyzed Selective N-Arylation of Oxadiazolones by Diaryliodonium Salts

  • Original language description

    Here, we report the method for copper-catalyzed N-arylation of diverse oxadiazolones by diaryliodonium salts under mild conditions in high yields (up to 92%) using available CuI as a catalyst. The developed method allows utilizing both symmetric and unsymmetric diaryliodonium salts bearing auxiliary groups such as 2,4,6-trimethoxyphenyl (TMP). We found that the steric effects in aryl moieties determined the chemoselectivity of N- and O-arylation of the 1,2,4-oxadiazol-5(4H)-ones. Mesityl-substituted diaryliodonium salts demonstrated the high potential as a selective arylation reagent. The structural study suggests that steric accessibility of N-atom in 1,2,4-oxadiazol-5(4H)-ones impact to arylation with sterically hindered diaryliodonium salts. The synthetic application of proposed method was also demonstrated on selective arylation of 1,3,4-oxadiazol-2(3H)-ones and 1,2,4-oxadiazole-5-thiol. (Figure presented.). © 2021 Wiley-VCH GmbH

  • 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

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2021

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    ADVANCED SYNTHESIS &amp; CATALYSIS

  • ISSN

    1615-4150

  • e-ISSN

  • Volume of the periodical

    363

  • Issue of the periodical within the volume

    14

  • Country of publishing house

    DE - GERMANY

  • Number of pages

    11

  • Pages from-to

    3566-3576

  • UT code for WoS article

    000658836300001

  • EID of the result in the Scopus database

    2-s2.0-85107761429