Ligand-free Ullmann-type arylation of oxazolidinones by diaryliodonium salts

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22310%2F23%3A43934046" target="_blank" >RIV/60461373:22310/23:43934046 - isvavai.cz</a>
Result on the web
<a href="http://DOI" target="_blank" >http://DOI</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1039/d2ob02122f" target="_blank" >10.1039/d2ob02122f</a>

Result language
angličtina
Original language name
Ligand-free Ullmann-type arylation of oxazolidinones by diaryliodonium salts
Original language description
The arylation of azaheterocycles can be considered as one of the most important processes for the preparation of various biologically active compounds. In the present work, we describe a method for the copper-catalyzed N-arylation of hindered oxazolidinones using diaryliodonium salts. The method succeeds in good to excellent yields for the arylation of 4-alkyloxazolidinones, including sterically hindered isopropyl- and tert-butyl-substituted. The efficiency of the method was demonstrated for a wide range of diaryliodonium salts - symmetric and unsymmetric as well as ortho-substituted derivatives. The developed approach will provide an important contribution in the development and preparation of novel drugs and bioactive molecules containing oxazolidinone moieties. © 2023 The Royal Society of Chemistry.
Czech name
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Czech description
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Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
10401 - Organic chemistry

Project
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Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Publication year
2023
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

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