Enantiopure isoindolinones through Viedma ripening

Chemistry. 2014 Oct 13;20(42):13527-30. doi: 10.1002/chem.201404320. Epub 2014 Aug 28.

Abstract

Here we demonstrate that deracemization of isoindolinones using Viedma ripening is possible starting from a racemic mixture of conglomerate crystals. Crystals of the enantiopure isoindolinones lose their chiral identity upon dissolution even without the need for a catalyst. This enabled complete deracemization of the reported isoindolinones without a catalyst.

Keywords: asymmetric amplification; chiral resolution; chirality; grinding; heterocycles.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Crystallization
  • Isoindoles / chemistry*
  • Solubility
  • Stereoisomerism

Substances

  • Isoindoles