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N-Heterocyclic Carbene-Catalyzed [3 + 3] Annulation of 5-Aminopyrazoles with Enals: Enantioselective Synthesis of Pyrazolo[3,4-b]pyridones.
Li, Jiahan; Duan, Xiao-Yong; Ren, Xiaojie; Li, Yanting; Qi, Jing.
Afiliação
  • Li J; College of Chemistry and Materials Science, Chemical Biology Key Laboratory of Hebei Province, Key Laboratory of Medicinal Chemistry and Molecular Diagnosis of the Ministry of Education, Hebei University, Baoding 071002, China.
  • Duan XY; College of Chemistry and Materials Science, Chemical Biology Key Laboratory of Hebei Province, Key Laboratory of Medicinal Chemistry and Molecular Diagnosis of the Ministry of Education, Hebei University, Baoding 071002, China.
  • Ren X; State Key Laboratory of New Pharmaceutical Preparations and Excipients, College of Chemistry and Materials Science, Hebei University, Baoding 071002, China.
  • Li Y; College of Chemistry and Materials Science, Chemical Biology Key Laboratory of Hebei Province, Key Laboratory of Medicinal Chemistry and Molecular Diagnosis of the Ministry of Education, Hebei University, Baoding 071002, China.
  • Qi J; College of Chemistry and Materials Science, Chemical Biology Key Laboratory of Hebei Province, Key Laboratory of Medicinal Chemistry and Molecular Diagnosis of the Ministry of Education, Hebei University, Baoding 071002, China.
J Org Chem ; 88(23): 16621-16632, 2023 Dec 01.
Article em En | MEDLINE | ID: mdl-37967027
ABSTRACT
An enantioselective construction of pyrazolo[3,4-b]pyridones was achieved via N-heterocyclic carbene-catalyzed [3 + 3] annulation of enals with 5-aminopyrazoles. This protocol not only offers a highly efficient synthetic approach for the preparation of various substituted pyrazolo[3,4-b]pyridones but also provides an effective method for the rapid synthesis of enantiopure spirooxindone derivatives.

Texto completo: 1 Coleções: 01-internacional 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 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Org Chem Ano de publicação: 2023 Tipo de documento: Article País de afiliação: China