Your browser doesn't support javascript.
loading
Cu-Mediated Stereoselective [4+2] Annulation between N-Hydroxybenzimidoyl Cyanide and Norbornene.
Liu, Kui; Chen, Zhen-Bang; Zhang, Fang-Ling; Tao, Shou-Wei; Xu, Qiong-Ming; Zhu, Yong-Ming.
Afiliação
  • Liu K; College of Pharmaceutical Sciences , Soochow University , Suzhou 215123 , China.
  • Chen ZB; College of Pharmaceutical Sciences , Soochow University , Suzhou 215123 , China.
  • Zhang FL; College of Pharmaceutical Sciences , Soochow University , Suzhou 215123 , China.
  • Chun Qian; College of Pharmaceutical Sciences , Soochow University , Suzhou 215123 , China.
  • Tao SW; College of Pharmaceutical Sciences , Soochow University , Suzhou 215123 , China.
  • Xu QM; College of Pharmaceutical Sciences , Soochow University , Suzhou 215123 , China.
  • Zhu YM; College of Pharmaceutical Sciences , Soochow University , Suzhou 215123 , China.
J Org Chem ; 83(15): 8457-8463, 2018 08 03.
Article em En | MEDLINE | ID: mdl-29905071
A Cu-mediated stereoselective [4+2] annulation between N-hydroxybenzimidoyl cyanides and norbornene (NBE) has been developed for the synthesis of 4 H-1,2-oxazin-4-ones. The reaction proceeds through sequentially forming C-O/C-C bonds. The advantage of this reaction includes high stereoselectivity, excellent yields, as well as simple and mild reaction conditions. A total of 26 examples are presented along with some control experiments.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article