Literature DB >> 25168197

Enantiopure isoindolinones through Viedma ripening.

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.
© 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

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

Mesh:

Substances:

Year:  2014        PMID: 25168197     DOI: 10.1002/chem.201404320

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  2 in total

1.  Influence of Ostwald's Rule of Stages in the Deracemization of a Compound Using a Racemic Resolving Agent.

Authors:  Tharit Lerdwiriyanupap; Giuseppe Belletti; Paul Tinnemans; Ruel Cedeno; Hugo Meekes; Elias Vlieg; Adrian E Flood
Journal:  Cryst Growth Des       Date:  2022-01-24       Impact factor: 4.076

2.  Role of Additives during Deracemization Using Temperature Cycling.

Authors:  Giuseppe Belletti; Hugo Meekes; Floris P J T Rutjes; Elias Vlieg
Journal:  Cryst Growth Des       Date:  2018-10-02       Impact factor: 4.076

  2 in total

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