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Enantioselective Friedel-Crafts Alkylation Reaction of Pyrroles with N -Unprotected Alkynyl Trifluoromethyl Ketimines.

Tatsuhiro UchikuraKureha ArugaRiku SuzukiTakahiko Akiyama
Published in: Organic letters (2022)
Developed herein is an enantioselective Friedel-Crafts alkylation reaction of N -unprotected alkynyl trifluoromethyl ketimines with pyrroles catalyzed by chiral phosphoric acid to furnish chiral primary α-trifluoromethyl-α-(2-pyrrolyl)propargylamines with high enantioselectivity. Transformation of the alkynyl group of the adducts afforded optically active α-trifluoromethylated amines bearing various substituents such as alkyl, alkenyl, enyne, and triazole without loss of optical purity.
Keyphrases
  • ionic liquid
  • capillary electrophoresis
  • room temperature
  • mass spectrometry