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CuH-Catalyzed Reductive Coupling of Nitroarenes with Phosphine Oxides for the Direct Synthesis of Phosphamides.
Tang, Jie; Li, Zhiyou; Meng, Qi; Liu, Long; Huang, Tianzeng; Li, Chunya; Li, Qiang; Chen, Tieqiao.
Afiliación
  • Tang J; Hainan Provincial Key Laboratory of Fine Chemical, School of Chemistry and Chemical Engineering, Hainan University, Haikou, Hainan 570228, China.
  • Li Z; Hainan Provincial Key Laboratory of Fine Chemical, School of Chemistry and Chemical Engineering, Hainan University, Haikou, Hainan 570228, China.
  • Meng Q; Hainan Provincial Key Laboratory of Fine Chemical, School of Chemistry and Chemical Engineering, Hainan University, Haikou, Hainan 570228, China.
  • Liu L; Hainan Provincial Key Laboratory of Fine Chemical, School of Chemistry and Chemical Engineering, Hainan University, Haikou, Hainan 570228, China.
  • Huang T; Hainan Provincial Key Laboratory of Fine Chemical, School of Chemistry and Chemical Engineering, Hainan University, Haikou, Hainan 570228, China.
  • Li C; Hainan Provincial Key Laboratory of Fine Chemical, School of Chemistry and Chemical Engineering, Hainan University, Haikou, Hainan 570228, China.
  • Li Q; Shandong Provincial Key Laboratory of Chemical Energy Storage and Novel Cell Technology, School of Chemistry and Chemical Engineering, Liaocheng University, No. 1, Hunan Street, Liaocheng, Shandong 252000, China.
  • Chen T; Hainan Provincial Key Laboratory of Fine Chemical, School of Chemistry and Chemical Engineering, Hainan University, Haikou, Hainan 570228, China.
J Org Chem ; 89(11): 7848-7858, 2024 Jun 07.
Article en En | MEDLINE | ID: mdl-38809686
ABSTRACT
A CuH-catalyzed reductive coupling of nitroarenes with phosphine oxides is developed, which produces a series of phosphamides in moderate to excellent yields with good functional group tolerance. Gram-scale synthesis and late-stage modification of nitro-aromatic functional molecule niclosamide are also successfully conducted. The mechanism study shows that the nitro group is transformed after being reduced to nitroso and a nucleophilic addition procedure is involved during the reaction.

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: J Org Chem Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: J Org Chem Año: 2024 Tipo del documento: Article País de afiliación: China