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Electrochemically Enabled Cascade Cyclization Reaction of Aromatic Aldehydes and Pyrazol-5-amines: Synthesis of Bis-pyrazolo[3,4-b:4',3'-e]pyridines.
Qian, Peng; Jiang, Shan; Fan, Hua; Jiang, Siqi; Xu, Longlong; Liu, Jiaojiao.
Afiliação
  • Qian P; School of Chemistry and Material Engineering, Engineering Research Center of Biomass Conversion and Pollution Prevention of Anhui Educational Institutions, Fuyang Normal University, Fuyang, Anhui 236037, P.R. China.
  • Jiang S; Experimental and Training Management Center, Fuyang Normal University, Fuyang, Anhui 236037, P.R. China.
  • Fan H; School of Chemistry and Material Engineering, Engineering Research Center of Biomass Conversion and Pollution Prevention of Anhui Educational Institutions, Fuyang Normal University, Fuyang, Anhui 236037, P.R. China.
  • Jiang S; School of Chemistry and Material Engineering, Engineering Research Center of Biomass Conversion and Pollution Prevention of Anhui Educational Institutions, Fuyang Normal University, Fuyang, Anhui 236037, P.R. China.
  • Xu L; School of Chemistry and Material Engineering, Engineering Research Center of Biomass Conversion and Pollution Prevention of Anhui Educational Institutions, Fuyang Normal University, Fuyang, Anhui 236037, P.R. China.
  • Liu J; School of Chemistry and Material Engineering, Engineering Research Center of Biomass Conversion and Pollution Prevention of Anhui Educational Institutions, Fuyang Normal University, Fuyang, Anhui 236037, P.R. China.
J Org Chem ; 87(14): 9242-9249, 2022 Jul 15.
Article em En | MEDLINE | ID: mdl-35795996
ABSTRACT
A facile method for the synthesis of bis-pyrazolo[3,4-b4',3'-e]pyridines from easily available aromatic aldehydes and pyrazol-5-amines was developed via electrochemistry. The reaction proceeded smoothly under metal and external chemical oxidant-free conditions, giving a variety of bis-pyrazolo[3,4-b4',3'-e]pyridines in moderate yields.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article