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Copper-Catalyzed Regioselective C-H Sulfonyloxylation of Electron-Rich Arenes with p-Toluenesulfonic Acid and Sulfonyloxylation of Aryl(mesityl)iodonium Sulfonates.
Huang, He; Wu, Yang; Zhang, Wen; Feng, Chun; Wang, Bi-Qin; Cai, Wan-Fei; Hu, Ping; Zhao, Ke-Qing; Xiang, Shi-Kai.
Afiliação
  • Huang H; College of Chemistry and Materials Science, Sichuan Normal University , Chengdu 610068, People's Republic of China.
  • Wu Y; College of Chemistry and Materials Science, Sichuan Normal University , Chengdu 610068, People's Republic of China.
  • Zhang W; College of Chemistry and Materials Science, Sichuan Normal University , Chengdu 610068, People's Republic of China.
  • Feng C; College of Chemistry and Materials Science, Sichuan Normal University , Chengdu 610068, People's Republic of China.
  • Wang BQ; College of Chemistry and Materials Science, Sichuan Normal University , Chengdu 610068, People's Republic of China.
  • Cai WF; College of Chemistry and Materials Science, Sichuan Normal University , Chengdu 610068, People's Republic of China.
  • Hu P; College of Chemistry and Materials Science, Sichuan Normal University , Chengdu 610068, People's Republic of China.
  • Zhao KQ; College of Chemistry and Materials Science, Sichuan Normal University , Chengdu 610068, People's Republic of China.
  • Xiang SK; College of Chemistry and Materials Science, Sichuan Normal University , Chengdu 610068, People's Republic of China.
J Org Chem ; 82(6): 3094-3101, 2017 03 17.
Article em En | MEDLINE | ID: mdl-28230367
ABSTRACT
Copper-catalyzed regioselective C-H sulfonyloxylation of electron-rich arenes with p-toluenesulfonic acid has been developed. Electron-rich benzene derivatives and heteroarenes can undergo this C-H sulfonyloxylation reaction to generate aryl tosylates. Furthermore, sulfonyloxylation of aryl(mesityl)iodonium sulfonates has also been investigated. Both aryl(mesityl)iodonium tosylates and triflates can react smoothly to get aryl sulfonates. The formed aryl sulfonates can be converted to phenols, as well as used as good partners of cross-coupling reactions.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Org Chem Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Org Chem Ano de publicação: 2017 Tipo de documento: Article