Application of Crystallization Inhibitors to Chiral Separations. 1. Design of Additives to Discriminate between the Racemic Compound and the Pure Enantiomer of Mandelic Acid-Reference-Cited by-同舟云学术

Application of Crystallization Inhibitors to Chiral Separations. 1. Design of Additives to Discriminate between the Racemic Compound and the Pure Enantiomer of Mandelic Acid

Published:2007-01-05 Issue:2 Volume:7 Page:218-224
ISSN:1528-7483
Container-title:Crystal Growth & Design
language:en
Short-container-title:Crystal Growth & Design

Author:

Mughal R. K.¹,Davey R. J.¹,Blagden N.¹

Affiliation:

1. The Molecular Materials Centre, School of Chemical Engineering and Analytical Sciences, University of Manchester, Sackville Street, Manchester M60 1QD, UK, and School of Pharmacy, University of Bradford, Bradford BD7 1DP, UK

Publisher

American Chemical Society (ACS)

Subject

Condensed Matter Physics,General Materials Science,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/cg0605638

Reference20 articles.

1. Jacques, J.; Collett, A.; Wilsen, S. H.Enantiomers, Racemates andResolutions; John Wiley and Sons Inc. New York, 1994.

2. On the validity of Wallach's rule: on the density and stability of racemic crystals compared with their chiral counterparts

3. Toward Stereochemical Control, Monitoring, and Understanding of Crystal Nucleation

4. Binary and ternary phase diagrams of two enantiomers in solvent systems

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