A FACILE APPROACH TO α,β-UNSATURATED LACTAMS BY RING-CLOSING METATHESIS

Авторы

  • Humaira Yasmeen Gondal Department of Chemistry, University of Sargodha
  • Didier Buisson Museum National d'Histoire Naturelle

DOI:

https://doi.org/10.1007/3044

Ключевые слова:

α, β-unsaturated lactams, Grubbs catalyst, ring-closing metathesis

Аннотация

A facile and efficient strategy for the synthesis of α,β-unsaturated lactams through ring-closing metathesis of easily prepared diene amides is being reported here. Reaction conditions were optimized for metathetic cyclization of diene amides to obtain five- to seven-membered unsubstituted and β-substituted α,β-unsaturated lactams in good to excellent yield.

How to Cite
Gondal, H. Y.; Buisson, D. Chem. Heterocycl. Compd. 2016, 52, 183. [Khim. Geterotsikl. Soedin. 2016, 52, 183.]

For this article in the English edition see DOI 10.1007/s10593-016-1858-y

Биография автора

Humaira Yasmeen Gondal, Department of Chemistry, University of Sargodha

Assistant Professor

Department of Chemistry, University of Sargodha, Sargodha, Pakistan

 

Загрузки

Опубликован

2016-04-11

Выпуск

Том 52 № 3 (2016)

Раздел

Оригинальные статьи