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Ligand-free Ullmann-type Arylation of Oxazolidinones by Diaryliodonium Salts Научная публикация

Журнал Organic and Biomolecular Chemistry
ISSN: 1477-0520 , E-ISSN: 1477-0539
Вых. Данные Год: 2023, Том: 21, Номер: 9, Страницы: 1952-1957 Страниц : 6 DOI: 10.1039/d2ob02122f
Авторы Podrezova Ekaterina V. 1 , Okhina Alina A. 2,3 , Rogachev Artem D. 2,3 , Baykov Sergey 4,1 , Kirschning Andreas 5 , Yusubov Mekhman 1 , Soldatova Natalia S. 1 , Postnikov Pavel S 6,1
Организации
1 Research School of Chemistry and Applied Biomedical Sciences, Tomsk Polytechnic University, Tomsk 634034, Russia
2 N. N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, acad. Lavrentiev ave., 9, Novosibirsk 630090, Russia
3 Novosibirsk State University, Pirogov str., 2, Novosibirsk 630090, Russia
4 Institute of Chemistry, Saint Petersburg State University, Saint Petersburg 199034, Russia
5 Leibniz University Hannover, Schneiderberg 1B, 30167 Hannover, Germany
6 Department of Solid State Engineering, Institute of Chemical Technology, Prague 16628, Czech Republic

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
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
Цитирование в БД:
БД Цитирований
OpenAlex 5
Web of science 6
Scopus 5
Альметрики: