| Literature DB >> 25168197 |
René R E Steendam1, Maxime C T Brouwer, Evelien M E Huijs, Michaël W Kulka, Hugo Meekes, Willem J P van Enckevort, Jan Raap, Floris P J T Rutjes, Elias Vlieg.
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.Entities:
Keywords: asymmetric amplification; chiral resolution; chirality; grinding; heterocycles
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Year: 2014 PMID: 25168197 DOI: 10.1002/chem.201404320
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236