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The influence of the substituent position in monocarboxymethyl-γ-cyclodextrins on enantioselectivity in capillary electrophoresis.
J Sep Sci. 2014 Oct;37(19):2779-84. doi: 10.1002/jssc.201400604. Epub 2014 Aug 20.
J Sep Sci. 2014.
PMID: 25047151
Influence of substituent position and cavity size of the regioisomers of monocarboxymethyl-α-, β-, and γ-cyclodextrins on the apparent stability constants of their complexes with both enantiomers of Tröger's base.
Řezanka P, Řezanková K, Sedláčková H, Mašek J, Rokosová L, Bláhová M, Řezanka M, Jindřich J, Sýkora D, Král V.
Řezanka P, et al. Among authors: rezankova k.
J Sep Sci. 2016 Mar;39(5):980-5. doi: 10.1002/jssc.201500845. Epub 2016 Jan 15.
J Sep Sci. 2016.
PMID: 26695522
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