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Catalyst-Free Electrochemical Sulfonylation of Organoboronic Acids.
Yao, Weiwei; Lv, Kang; Xie, Zixi; Qiu, Hui; Ma, Mengtao.
Afiliação
  • Yao W; College of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210023, China.
  • Lv K; College of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210023, China.
  • Xie Z; College of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210023, China.
  • Qiu H; Department of Chemistry and Material Science, College of Science, Nanjing Forestry University, Nanjing 210037, China.
  • Ma M; Department of Chemistry and Material Science, College of Science, Nanjing Forestry University, Nanjing 210037, China.
J Org Chem ; 88(4): 2296-2305, 2023 Feb 17.
Article em En | MEDLINE | ID: mdl-36727513
ABSTRACT
A simple and efficient electrochemical sulfonylation of organoboronic acids with sodium arylsulfinate salts has been reported for the first time. A variety of aryl, heteroaryl, and alkenylsulfones were obtained in good to excellent yields via a simple electrochemical sulfonylation of various arylboronic acids, heterocyclic boronic acids, or alkenylboronic acids with sodium arylsulfinate at room temperature in 5 h under the catalyst-free and additive-free conditions. A plausible mechanism has been proposed based on various radical-trapping and CV control experiments.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: J Org Chem Ano de publicação: 2023 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: J Org Chem Ano de publicação: 2023 Tipo de documento: Article País de afiliação: China