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Construction of Trisubstituted Hydrazones via Base-Mediated Cascade Condensation N-Alkylation.
Hao, Wentao; Gao, Shuo; Cui, Hongyi; Ding, Ding; Jiang, Shaohua; Zhang, Chunyan; Ji, Yuqi; Zhang, Guoying.
Afiliação
  • Hao W; State Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan 030001, China.
  • Gao S; College of Ecology, Taiyuan University of Technology, Taiyuan 030001, China.
  • Cui H; University of Chinese Academy of Sciences, Beijing 100049, China.
  • Ding D; State Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan 030001, China.
  • Jiang S; University of Chinese Academy of Sciences, Beijing 100049, China.
  • Zhang C; State Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan 030001, China.
  • Ji Y; University of Chinese Academy of Sciences, Beijing 100049, China.
  • Zhang G; State Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan 030001, China.
J Org Chem ; 89(4): 2605-2621, 2024 Feb 16.
Article em En | MEDLINE | ID: mdl-38315164
ABSTRACT
A practical base-promoted tandem condensation N-alkylation reaction for the formation of trisubstituted hydrazones has been developed employing aldehydes and hydrazines with alkyl halides. Crucially, this reaction successfully overcomes chemoselectivity problems, allowing for the reaction of multiple components in a one-pot manner. Halo- and heterofunctional groups, as well as free hydroxyl and amino groups, are tolerated in this transformation to produce a wide range of trisubstituted hydrazones in good to excellent yields.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Org Chem Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Org Chem Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China