Issue 9, 2011
From the journal:

Chemical Communications

Quininium mandelates—a systematic study of chiral discrimination in crystals of diastereomeric salts†

Nikoletta B. Báthori,*a   Luigi R. Nassimbenia  and  Clive L. Oliverb  

* Corresponding authors

a Centre for Crystal Engineering, Department of Chemistry, Cape Peninsula University of Technology, P.O. Box 652, Cape Town, South Africa
E-mail: bathorin@cput.ac.za
Fax: +27 21 460 3854
Tel: +27 21 460 8354

b Centre for Supramolecular Chemistry Research, Department of Chemistry, University of Cape Town, South Africa

Abstract

The selectivity profile for the resolution of mandelic acid by quinine is dominated by structures comprising (QUIN+)(MAND−) salts with Z′ = 3 which contain (R)-, (R)- and (S)-mandelate anions.

Graphical abstract: Quininium mandelates—a systematic study of chiral discrimination in crystals of diastereomeric salts

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Article information

DOI
https://doi.org/10.1039/C0CC04279J
Article type
Communication
Submitted
07 Oct 2010
Accepted
10 Dec 2010
First published
12 Jan 2011

Chem. Commun., 2011,47, 2670-2672

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Quininium mandelates—a systematic study of chiral discrimination in crystals of diastereomeric salts

N. B. Báthori, L. R. Nassimbeni and C. L. Oliver, Chem. Commun., 2011, 47, 2670 DOI: 10.1039/C0CC04279J

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