Structural Analysis of d-Phenylglycinamide Salts Uncovers Potential Pitfalls in Chiral Resolution via Diastereomeric Salt Formation
Author:
Affiliation:
1. IMCN Institute of Condensed Matter and Nanosciences, Université catholique de Louvain, Place Louis Pasteur 1, 1348 Louvain-la-Neuve, Belgium
2. Chemistry Department, University of Namur, Rue de Bruxelles 61, 5000 Namur, Belgium
Funder
Universit? Catholique de Louvain
Fonds De La Recherche Scientifique - FNRS
Publisher
American Chemical Society (ACS)
Subject
Condensed Matter Physics,General Materials Science,General Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.cgd.8b01769
Reference57 articles.
1. Enantiomer Separation
2. Preferential Crystallization
3. Pitfalls and rewards of preferential crystallization
4. Observation of Efficient Preferential Enrichment Phenomenon for a Cocrystal of (dl)-Phenylalanine and Fumaric Acid under Nonequilibrium Crystallization Conditions
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