Ligand-free Ullmann-type Arylation of Oxazolidinones by Diaryliodonium Salts Научная публикация
Журнал |
Organic and Biomolecular Chemistry
ISSN: 1477-0520 , E-ISSN: 1477-0539 |
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Вых. Данные | Год: 2023, Том: 21, Номер: 9, Страницы: 1952-1957 Страниц : 6 DOI: 10.1039/d2ob02122f | ||||||||||||
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Реферат:
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.
Библиографическая ссылка:
Podrezova E.V.
, Okhina A.A.
, Rogachev A.D.
, Baykov S.
, Kirschning A.
, Yusubov M.
, Soldatova N.S.
, Postnikov P.S.
Ligand-free Ullmann-type Arylation of Oxazolidinones by Diaryliodonium Salts
Organic and Biomolecular Chemistry. 2023. V.21. N9. P.1952-1957. DOI: 10.1039/d2ob02122f WOS Scopus CAPlusCA PMID OpenAlex
Ligand-free Ullmann-type Arylation of Oxazolidinones by Diaryliodonium Salts
Organic and Biomolecular Chemistry. 2023. V.21. N9. P.1952-1957. DOI: 10.1039/d2ob02122f WOS Scopus CAPlusCA PMID OpenAlex
Даты:
Поступила в редакцию: | 22 нояб. 2022 г. |
Принята к публикации: | 6 февр. 2023 г. |
Опубликована online: | 6 февр. 2023 г. |
Опубликована в печати: | 7 мар. 2023 г. |
Идентификаторы БД:
Web of science: | WOS:000931652900001 |
Scopus: | 2-s2.0-85148677194 |
Chemical Abstracts: | 2023:302508 |
Chemical Abstracts (print): | 182:48133 |
PMID (PubMed): | 36757159 |
OpenAlex: | W4319316443 |