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Visible-Light-Mediated Anti-Regioselective Nitrone 1,3-Dipolar Cycloaddition Reaction and Synthesis of Bisindolylmethanes.
Zheng, Lewei; Gao, Fei; Yang, Chao; Gao, Guo-Lin; Zhao, Yating; Gao, Yuan; Xia, Wujiong.
Afiliação
  • Zheng L; State Key Lab of Urban Water Resource and Environment, Harbin Institute of Technology (Shenzhen) , Shenzhen 518055, China.
  • Gao F; State Key Lab of Urban Water Resource and Environment, Harbin Institute of Technology (Shenzhen) , Shenzhen 518055, China.
  • Yang C; State Key Lab of Urban Water Resource and Environment, Harbin Institute of Technology (Shenzhen) , Shenzhen 518055, China.
  • Gao GL; State Key Lab of Urban Water Resource and Environment, Harbin Institute of Technology (Shenzhen) , Shenzhen 518055, China.
  • Zhao Y; State Key Lab of Urban Water Resource and Environment, Harbin Institute of Technology (Shenzhen) , Shenzhen 518055, China.
  • Gao Y; School of Chemistry and Chemical Engineering, Yantai University , #30 Qingquan Road, Laishan District, Yantai 264005, China.
  • Xia W; State Key Lab of Urban Water Resource and Environment, Harbin Institute of Technology (Shenzhen) , Shenzhen 518055, China.
Org Lett ; 19(19): 5086-5089, 2017 10 06.
Article em En | MEDLINE | ID: mdl-28920699
ABSTRACT
The development of photoredox reactions of 1,3-dipolar cycloaddition of nitrones with alkenes is reported. It offers an efficient synthetic method to obtain isoxazolidine derivatives under mild conditions in synthetically useful yields. The nitrones are cyclized with oxidizable styrenes and aliphatic alkenes via a polar radical crossover cycloaddition reaction through photocatalytic reaction without additives. In addition, bis(indole)methanes can also be prepared through this method.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article