| Literature DB >> 31393026 |
Ryusei Oketani1, Francesco Marin2, Paul Tinnemans3, Marine Hoquante1, Anne Laurent2, Clément Brandel1, Pascal Cardinael1, Hugo Meekes3, Elias Vlieg3, Yves Geerts2, Gérard Coquerel1.
Abstract
A productive deracemization process based on a quaternary phase diagram study of a naphthamide derivative is reported. New racemic compounds of an atropisomeric naphthamide derivative have been discovered, and a quaternary phase diagram has been constructed that indicated that four solids are stable in a methanol/H2 O solution. Based on the results of a heterogeneous equilibria study showing the stable domain of the conglomerate, a second-order asymmetric transformation was achieved with up to 97 % ee. Furthermore, this methodology showcases the chiral separation of a stable racemic compound forming system and does not suffer from any of the typical limitations of deracemization, although application is still limited to conglomerate-forming systems. We anticipate that this present study will serve as a fundamental model for the design of sophisticated chiral separation processes.Entities:
Keywords: atropisomerism; chiral resolution; deracemization; phase diagrams; second-order asymmetric transformation
Year: 2019 PMID: 31393026 DOI: 10.1002/chem.201903338
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236