Login / Signup

Dinuclear zinc-catalyzed asymmetric Friedel-Crafts alkylation/cyclization of 3-aminophenols with α,α-dicyanoolefins.

Hang YanShi-Kun JiaYu-Huan GengJiao-Jiao HanYuan-Zhao HuaMin-Can Wang
Published in: Chemical communications (Cambridge, England) (2021)
An enantioselective Friedel-Crafts alkylation/cyclization tandem reaction of 3-aminophenols with α,α-dicyanoolefins has been performed successfully using a chiral dinuclear zinc catalyst, leading to a range of chiral 2-amino-4H-chromenes (up to 98% yield and >99% ee). To the best of our knowledge, this is the first asymmetric example of the dinuclear zinc-catalysed functionalization of aromatic C(sp2)-H bonds.
Keyphrases
  • oxide nanoparticles
  • ionic liquid
  • room temperature
  • healthcare
  • solid state
  • highly efficient
  • amino acid
  • reduced graphene oxide
  • carbon dioxide