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	1.	The influence of the substituent position in monocarboxymethyl-γ-cyclodextrins on enantioselectivity in capillary electrophoresis. [electronic resource] by Rezanka, Pavel Rokosová, Lenka Rezanková, Klára Bláhová, Markéta Rezanka, Michal Sýkora, David Jindřich, Jindřich Král, Vladimír Producer: 20150521 In: Journal of separation science vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	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. [electronic resource] by Řezanka, Pavel Řezanková, Klára Sedláčková, Helena Mašek, Jindřich Rokosová, Lenka Bláhová, Markéta Řezanka, Michal Jindřich, Jindřich Sýkora, David Král, Vladimír Producer: 20160706 In: Journal of separation science vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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