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Electro-oxidative three-component cascade coupling of isocyanides with elemental sulfur and amines for the synthesis of 2-aminobenzothiazoles.
Huang, Peng-Fei; Fu, Jia-Le; Peng, Ying; Fan, Jian-Hong; Zhong, Long-Jin; Tang, Ke-Wen; Liu, Yu.
Afiliação
  • Huang PF; Department of Chemistry and Chemical Engineering, Hunan Institute of Science and Technology, Yueyang 414006, China. pengfeihuang@whu.edu.cn.
  • Fu JL; Department of Chemistry and Chemical Engineering, Hunan Institute of Science and Technology, Yueyang 414006, China. pengfeihuang@whu.edu.cn.
  • Peng Y; Department of Chemistry and Chemical Engineering, Hunan Institute of Science and Technology, Yueyang 414006, China. pengfeihuang@whu.edu.cn.
  • Fan JH; Department of Chemistry and Chemical Engineering, Hunan Institute of Science and Technology, Yueyang 414006, China. pengfeihuang@whu.edu.cn.
  • Zhong LJ; Department of Chemistry and Chemical Engineering, Hunan Institute of Science and Technology, Yueyang 414006, China. pengfeihuang@whu.edu.cn.
  • Tang KW; Department of Chemistry and Chemical Engineering, Hunan Institute of Science and Technology, Yueyang 414006, China. pengfeihuang@whu.edu.cn.
  • Liu Y; Department of Chemistry and Chemical Engineering, Hunan Institute of Science and Technology, Yueyang 414006, China. pengfeihuang@whu.edu.cn.
Org Biomol Chem ; 22(18): 3752-3760, 2024 May 08.
Article em En | MEDLINE | ID: mdl-38652536
ABSTRACT
2-Aminobenzothiazoles are commonly encountered in various functional compounds. Herein, we disclose an electro-oxidative three-component reaction for the effective synthesis of 2-aminobenzothiazoles under mild conditions, utilizing non-toxic and abundant elemental sulfur as the sulfur source. Both aliphatic amines and aryl amines demonstrate good compatibility at room temperature, highlighting the broad functional group tolerance of this approach. Additionally, elemental selenium demonstrated reactivities comparable to those of elemental sulfur.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article