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gem-Digold Acetylide Complexes for Catalytic Intermolecular [4 + 2] Cycloaddition: Having Two Gold Centers Is Better for Asymmetric Catalysis.
Nanko, Masaki; Shibuya, Satoru; Inaba, Yuya; Ono, Soichiro; Ito, Shigekazu; Mikami, Koichi.
Afiliação
  • Nanko M; Department of Chemical Science and Engineering, School of Materials and Chemical Technology , Tokyo Institute of Technology , Tokyo 152-8552 , Japan.
  • Shibuya S; Department of Chemical Science and Engineering, School of Materials and Chemical Technology , Tokyo Institute of Technology , Tokyo 152-8552 , Japan.
  • Inaba Y; Department of Chemical Science and Engineering, School of Materials and Chemical Technology , Tokyo Institute of Technology , Tokyo 152-8552 , Japan.
  • Ono S; Department of Chemical Science and Engineering, School of Materials and Chemical Technology , Tokyo Institute of Technology , Tokyo 152-8552 , Japan.
  • Ito S; Department of Chemical Science and Engineering, School of Materials and Chemical Technology , Tokyo Institute of Technology , Tokyo 152-8552 , Japan.
  • Mikami K; Department of Chemical Science and Engineering, School of Materials and Chemical Technology , Tokyo Institute of Technology , Tokyo 152-8552 , Japan.
Org Lett ; 20(23): 7353-7357, 2018 12 07.
Article em En | MEDLINE | ID: mdl-30277079
Gold(I)-catalyzed highly enantioselective intermolecular [4 + 2] cycloaddition is shown with ynones and cyclohexadiene. Various bicyclo[2.2.2]octadiene derivatives are produced in high yields (up to 99%) with good enantioselectivity (up to 96% ee). Key to the success is generation of the gem-digold terminal alkyne as a catalytic on-cycle species. As proof of the gem-digold catalysis, a positive nonlinear effect is clarified between the ee's of the ligand and the cycloadduct.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Org Lett Assunto da revista: BIOQUIMICA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Org Lett Assunto da revista: BIOQUIMICA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Japão