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Aziridine Opening via a Phenonium Ion Enables Synthesis of Complex Phenethylamine Derivatives.

Hannah M HolstJack T FloreancigCasey B RittsNicholas J Race
Published in: Organic letters (2021)
We report that the treatment of unsymmetrical 2,3-disubstituted aziridines with TiCl 4 yields β-phenethylamine products via the intermediacy of a phenonium ion. Derivatization of the products obtained via this method is demonstrated. Computational analysis of the reaction pathway provides insight into the reaction mechanism, including the selectivity of the phenonium opening.
Keyphrases
  • ms ms
  • high performance liquid chromatography
  • liquid chromatography
  • combination therapy
  • tandem mass spectrometry
  • structure activity relationship