Login / Signup

Catalytic Asymmetric Synthesis of Atropisomeric N -Aryl 1,2,4-Triazoles.

Sooyun ChoiMelody C GuoGavin M CoombsScott J Miller
Published in: The Journal of organic chemistry (2023)
The atroposelective synthesis of N -aryl 1,2,4-triazoles was developed. A cyclodehydration reaction was rendered asymmetric with the use of a chiral phosphoric acid catalyst to afford atropisomeric N -aryl 1,2,4-triazoles in up to 91:9 er. Recrystallization of the isolated heterocycle further enriched the atropisomeric ratio of several analogs to 99:1 er or greater. A divergent and substrate-dependent reaction pathway yielding a different heterocyclic product is also disclosed.
Keyphrases
  • ionic liquid
  • estrogen receptor
  • endoplasmic reticulum
  • breast cancer cells
  • room temperature
  • highly efficient
  • reduced graphene oxide
  • mass spectrometry
  • gold nanoparticles
  • capillary electrophoresis
  • crystal structure