Enantiopure Isoindolinones through Viedma Ripening

René R. E. Steendam, Maxime C. T. Brouwer, Evelien M. E. Huijs, Michael Kulka, Hugo Meekes, W.J.P. van Enckevort, Jan Raap, Floris P. J. T. Rutjes, Elias Vlieg

Chemistry - A European Journal · 2014 · 42 citations · 15 references

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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.

References

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