Simultaneous chiral resolution of two racemic compounds by preferential cocrystallization
Zhou, Fuli and Shemchuk, Oleksii and Charpentier, Maxime D. and Matheys, Chloé and Collard, Laurent and ter Horst, Joop H. and Leyssens, Tom (2021) Simultaneous chiral resolution of two racemic compounds by preferential cocrystallization. Angewandte Chemie - International Edition, 60 (37). pp. 20264-20268. ISSN 1521-3773 (https://doi.org/10.26434/chemrxiv.14730537.v1)
Preview |
Text.
Filename: Zhou_etal_ACIE_2021_Simultaneous_chiral_resolution_of_two_racemic_compounds.pdf
Accepted Author Manuscript Download (3MB)| Preview |
Abstract
We tap into an unexplored area of preferential crystallization, being the first to develop simultaneous chiral resolution of two racemic compounds by preferential cocrystallization. We highlight how the two racemic compounds RS-mandelic acid (MAN) and RS-etiracetam (ETI) can be combined together as enantiospecific R-MAN⋅R-ETI and S-MAN⋅S-ETI cocrystals forming a stable conglomerate system and subsequently develop a cyclic preferential crystallization allowing to simultaneous resolve both compounds. The developed process leads to excellent enantiopurity both for etiracetam (ee>98 %) and mandelic acid (ee≈95 %) enantiomers.
ORCID iDs
Zhou, Fuli, Shemchuk, Oleksii, Charpentier, Maxime D., Matheys, Chloé, Collard, Laurent, ter Horst, Joop H. ORCID: https://orcid.org/0000-0003-0118-2160 and Leyssens, Tom;-
-
Item type: Article ID code: 78134 Dates: DateEvent6 September 2021Published6 August 2021Published Online7 July 2021AcceptedNotes: A previous version of this manuscript has been deposited on a preprint server (https://doi.org/10.26434/chemrxiv.14730537.v1). Subjects: Science > Chemistry Department: Faculty of Science > Strathclyde Institute of Pharmacy and Biomedical Sciences Depositing user: Pure Administrator Date deposited: 12 Oct 2021 10:37 Last modified: 11 Nov 2024 13:11 Related URLs: URI: https://strathprints.strath.ac.uk/id/eprint/78134