Atropselective synthesis of N-aryl pyridones via dynamic kinetic resolution enabled by non-covalent interactions

Org Biomol Chem. 2022 Mar 23;20(12):2392-2396. doi: 10.1039/d2ob00177b.

Abstract

The dynamic kinetic resolution of C-N atropisomeric pyridones was achieved via asymmetric phase-transfer catalysis, exploiting a rotational barrier-lowering hydrogen bond in the starting materials. X-ray and NMR experiments revealed the presence of a barrier-raising ground state CH⋯π interaction in the product, supported by DFT calculations. A co-crystal of the quinidine-derived phase-transfer catalyst and substrate reveals key substrate-catalyst non-covalent interactions.

MeSH terms

  • Catalysis
  • Hydrogen Bonding
  • Kinetics
  • Magnetic Resonance Spectroscopy
  • Pyridones*

Substances

  • Pyridones