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[3 + 2] Cycloaddition of Nitrile Imines with Enamides: An Approach to Functionalized Pyrazolines and Pyrazoles.
Tu, Liang; Gao, Limei; Wang, Xiaomeng; Shi, Ruijie; Ma, Rupei; Li, Junfei; Lan, Xiaoshuang; Zheng, Yongsheng; Liu, Jikai.
Afiliação
  • Tu L; School of Pharmaceutical Sciences, South-Central University for Nationalities, Wuhan 430074, China.
  • Gao L; School of Pharmaceutical Sciences, South-Central University for Nationalities, Wuhan 430074, China.
  • Wang X; School of Pharmaceutical Sciences, South-Central University for Nationalities, Wuhan 430074, China.
  • Shi R; School of Pharmaceutical Sciences, South-Central University for Nationalities, Wuhan 430074, China.
  • Ma R; School of Pharmaceutical Sciences, South-Central University for Nationalities, Wuhan 430074, China.
  • Li J; School of Pharmaceutical Sciences, South-Central University for Nationalities, Wuhan 430074, China.
  • Lan X; School of Pharmaceutical Sciences, South-Central University for Nationalities, Wuhan 430074, China.
  • Zheng Y; School of Pharmaceutical Sciences, South-Central University for Nationalities, Wuhan 430074, China.
  • Liu J; School of Pharmaceutical Sciences, South-Central University for Nationalities, Wuhan 430074, China.
J Org Chem ; 86(1): 559-573, 2021 01 01.
Article em En | MEDLINE | ID: mdl-33301335
ABSTRACT
An efficient [3 + 2] cycloaddition of in situ generated nitrile imines with enamides has been established. A wide range of functionalized pyrazoline derivatives (53 examples) were obtained in moderate to good yields (up to 96%) under very mild conditions. This protocol features broad substrate scope, good functional group tolerance, and operational simplicity. Practical transformation of the products into useful pyrazoles via a one-pot process and the scalability of this protocol highlight the utility of this synthetic methodology.

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Guideline Idioma: En Revista: J Org Chem Ano de publicação: 2021 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Guideline Idioma: En Revista: J Org Chem Ano de publicação: 2021 Tipo de documento: Article País de afiliação: China