Your browser doesn't support javascript.
loading
Cascade reaction of o-enoyl arylisocyanide and o-hydroxy aromatic aldimine: diastereoselective access to a polycyclic spirobenzoxazine chromeno[4,3-b]pyrrole derivative.
Xiao, Yao; Peng, Xin; Shen, Jie; Cui, Lei; Lu, Shanya; Jia, Xueshun; Li, Chunju; Li, Jian.
Affiliation
  • Xiao Y; Department of Chemistry, College of Sciences & Institute for Sustainable Energy, Shanghai University, 99 Shangda Road, Shanghai 200444, P. R. China. cuilei@shu.edu.cn.
  • Peng X; Department of Chemistry, College of Sciences & Institute for Sustainable Energy, Shanghai University, 99 Shangda Road, Shanghai 200444, P. R. China. cuilei@shu.edu.cn.
  • Shen J; Department of Chemistry, College of Sciences & Institute for Sustainable Energy, Shanghai University, 99 Shangda Road, Shanghai 200444, P. R. China. cuilei@shu.edu.cn.
  • Cui L; Department of Chemistry, College of Sciences & Institute for Sustainable Energy, Shanghai University, 99 Shangda Road, Shanghai 200444, P. R. China. cuilei@shu.edu.cn.
  • Lu S; Department of Chemistry, College of Sciences & Institute for Sustainable Energy, Shanghai University, 99 Shangda Road, Shanghai 200444, P. R. China. cuilei@shu.edu.cn.
  • Jia X; Department of Chemistry, College of Sciences & Institute for Sustainable Energy, Shanghai University, 99 Shangda Road, Shanghai 200444, P. R. China. cuilei@shu.edu.cn.
  • Li C; Key Laboratory of Inorganic-Organic Hybrid Functional Material Chemistry, Ministry of Education, Tianjin Key Laboratory of Structure and Performance for Functional Molecules, College of Chemistry, Tianjin Normal University, Tianjin 300387, P. R. China.
  • Li J; Department of Chemistry, College of Sciences & Institute for Sustainable Energy, Shanghai University, 99 Shangda Road, Shanghai 200444, P. R. China. cuilei@shu.edu.cn.
Chem Commun (Camb) ; 58(75): 10528-10531, 2022 Sep 20.
Article in En | MEDLINE | ID: mdl-36043872
A series of structurally unusual spirobenzoxazine chromeno[4,3-b]pyrrole derivatives have been efficiently constructed in a single operation from readily available starting materials. This domino transformation forms successively three new rings and provides a fast and economic strategy with excellent diastereoselectivity.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pyrroles Language: En Journal: Chem Commun (Camb) Journal subject: QUIMICA Year: 2022 Document type: Article Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pyrroles Language: En Journal: Chem Commun (Camb) Journal subject: QUIMICA Year: 2022 Document type: Article Country of publication: United kingdom