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Synthesis of Unsymmetric Thiosulfonates Starting from N-Substituted O-Thiocarbamates: Easy Access to the S-SO2 Bond.
Yang, Cheng-Li; Gao, Xue-Jie; Jiang, Xin-Yi; Shi, Zhen; Hao, Er-Jun; Dong, Zhi-Bing.
Afiliação
  • Yang CL; School of Chemistry and Environmental Engineering, Wuhan Institute of Technology, Wuhan 430205, China.
  • Gao XJ; School of Chemistry and Environmental Engineering, Wuhan Institute of Technology, Wuhan 430205, China.
  • Jiang XY; School of Chemistry and Environmental Engineering, Wuhan Institute of Technology, Wuhan 430205, China.
  • Shi Z; Hubei Key Laboratory of Biologic Resources Protection and Utilization, Hubei Minzu University, Enshi 445000, China.
  • Hao EJ; School of Chemistry and Chemical Engineering, Henan Normal University, Xinxiang 453007, China.
  • Dong ZB; School of Chemistry and Environmental Engineering, Wuhan Institute of Technology, Wuhan 430205, China.
J Org Chem ; 87(17): 11656-11668, 2022 Sep 02.
Article em En | MEDLINE | ID: mdl-35959946
Using phenyliodine diacetate as an oxidant and nickel acetate as a promoter, a wide range of unsymmetric thiosulfonates could be furnished easily in moderate to excellent yields starting from N-substituted O-thiocarbamates and sodium sulfinates. This protocol features mild conditions, short reaction times, and high atomic utilization, which can provide an alternative method for the synthesis of unsymmetric thiosulfonates. In addition, the reaction could be scaled up on a gram scale, showing potential application value in industry.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article