One-pot preparation of piperazines by regioselective ring-opening of non-activated arylaziridines

Org Biomol Chem. 2012 Mar 14;10(10):1962-5. doi: 10.1039/c2ob07099e. Epub 2012 Jan 30.

Abstract

Herein we report a new straightforward synthesis of cis and trans 2,5-disubstituted N,N-dialkylpiperazines, even in enantioenriched form, by reacting non-activated N-alkyl arylaziridines in the presence of a catalytic amount of a Lewis acid. A stereochemical and NMR investigation revealed useful mechanistic insights for this process.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aziridines / chemical synthesis
  • Aziridines / chemistry*
  • Catalysis
  • Lewis Acids / chemistry
  • Magnetic Resonance Spectroscopy
  • Piperazines / chemical synthesis
  • Piperazines / chemistry*
  • Stereoisomerism

Substances

  • Aziridines
  • Lewis Acids
  • Piperazines