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Enantioselective Synthesis of Benzofuran-Fused N-Heterocycles via Chiral Squaramide Catalyzed [4 + 2] Cyclization of Azadienes with Azlactones.

Xiaoping LiJuzhang YanJialiang QinShilin LinWeiwen ChenRuoting ZhanHuicai Huang
Published in: The Journal of organic chemistry (2019)
An asymmetric cyclization reaction of azadienes and azlactones was investigated by employing a Cinchona squaramide catalyst, which could afford a series of benzofuran-fused six-membered heterocycles containing a α,α-disubstituted amino acid unit in a highly diastereoselective (>20:1 dr) and enantioselective (up to 99% ee) manner with good to excellent yields (up to 92%). A plausible pathway was proposed to explain the reaction process.
Keyphrases
  • amino acid
  • room temperature
  • ionic liquid
  • highly efficient
  • reduced graphene oxide
  • electron transfer
  • capillary electrophoresis
  • gold nanoparticles
  • visible light
  • solid state