Catalytic, asymmetric azidations at carbonyls: achiral and meso-anhydride desymmetrisation affords enantioenriched γ-lactams

Org Biomol Chem. 2022 Aug 17;20(32):6384-6393. doi: 10.1039/d2ob01040b.

Abstract

An unprecedented organocatalytic process involving the asymmetric addition of azide to meso-anhydrides has been developed, promoted by novel sulfamide-substituted Cinchona alkaloid-based catalysts. Readily available glutaric anhydrides can be smoothly converted to enantioenriched hemi-acyl azides and from there to either γ-amino acids or γ-lactams.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acids / chemistry
  • Anhydrides / chemistry
  • Azides
  • Catalysis
  • Cinchona Alkaloids* / chemistry
  • Lactams* / chemistry

Substances

  • Amino Acids
  • Anhydrides
  • Azides
  • Cinchona Alkaloids
  • Lactams