A Hybrid Mechanism in Chiral Discrimination Induced by Crystallization of Supramolecular Compounds
Author:
Affiliation:
1. Unité de Cristallogenèse, Sciences et Méthodes Séparatives (SMS) - UPRES EA 3233, IRCOF IMR 4114, Université de ROUEN, Rue Tesnière, F-76821 Mont Saint-Aignan Cedex, France
Publisher
American Chemical Society (ACS)
Subject
Materials Chemistry,Surfaces, Coatings and Films,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jp301708v
Reference56 articles.
1. aCoquerel, G.InTopics in Current Chemistry (Novel Optical Resolution Technologies;Sakai, K., Hirayama, N., Tamura, R., Eds.Springer:Berlin, Heidelberg, 2007; Vol.269, Chapter 1, pp1–50.
2. Dutch Resolution: Separationof Enantiomers with Families of Resolving Agents. A Status Report
3. Resolution of Enantiomers by Non-Conventional Methods
4. Study of the diastereoisomers formed between (N-alkyl)-pipecolic acid-anilides and 2R,3R-tartaric acid or O,O′-dibenzoyl-2R,3R-tartaric acid. Do the tartaric acids form molecular-complexes, instead of salts during optical resolutions?
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