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Nickel-Catalyzed Asymmetric Friedel-Crafts Propargylation of 3-Substituted Indoles with Propargylic Carbonates Bearing an Internal Alkyne Group.

Yusuke MiyazakiBiao ZhouHiroaki TsujiMotoi Kawatsura
Published in: Organic letters (2020)
The nickel-catalyzed highly enantioselective Friedel-Crafts propargylation of 3-substituted indoles with propargylic carbonates bearing an internal alkyne group was developed. A wide array of the propargylic carbonates as well as 3-substituted indoles can be applicable to the asymmetric nickel catalysis, providing the corresponding chiral C-3 propargylated indolenine derivatives bearing two vicinal chiral centers in up to 89% yield with up to >99% ee and 94:6 dr (24 examples).
Keyphrases
  • molecular docking
  • reduced graphene oxide
  • oxide nanoparticles
  • room temperature
  • carbon nanotubes
  • metal organic framework
  • ionic liquid
  • capillary electrophoresis
  • solid state
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