New Advances in the Synthetic Application of Enantiomeric 1-Phenylethylamine (α-PEA): Privileged Chiral Inducer and Auxiliary

Molecules. 2020 Oct 23;25(21):4907. doi: 10.3390/molecules25214907.

Abstract

New developments in the synthesis, resolution, and synthetic applications of chiral 1-phenylethylamine (α-PEA) reported in the last decade have been reviewed. In particular, improvements in the synthesis of α-PEA and its derivatives and chiral resolution, as well as their applications in the resolution of other compounds, were discussed. α-PEA was used as a chiral auxiliary in the diastereoselective synthesis of medicinal substances and natural products. Chiral ligands with α-PEA moieties were applied in asymmetric reactions, and effective modular chiral organocatalysts were constructed with α-PEA fragments and used in important synthetic reactions.

Keywords: 1-phenylethylamines; asymmetric synthesis; chiral auxiliary; chiral ligands; diastereoselectivity; modular organocatalysts; resolution; α-methylbenzylamine.

Publication types

  • Review

MeSH terms

  • Chemistry Techniques, Synthetic
  • Phenethylamines / chemical synthesis*
  • Phenethylamines / chemistry*
  • Stereoisomerism

Substances

  • Phenethylamines