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

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dc.contributor.authorŘezanka Pavelcs
dc.contributor.authorŘezanková Kláracs
dc.contributor.authorSedláčková Helenacs
dc.contributor.authorMašek Jindřichcs
dc.contributor.authorRokosová Lenkacs
dc.contributor.authorBláhová Markétacs
dc.contributor.authorŘezanka Michalcs
dc.contributor.authorJindřich Jindřichcs
dc.contributor.authorSýkora Davidcs
dc.contributor.authorKrál Vladimírcs
dc.date.accessioned2018-09-25T11:44:26Z
dc.date.available2018-09-25T11:44:26Z
dc.date.issued2016cs
dc.format.extent6cs
dc.identifier.doi10.1002/jssc.201500845
dc.identifier.issn1615-9306cs
dc.identifier.urihttps://dspace.tul.cz/handle/15240/26786
dc.language.isoengcs
dc.publisherWILEY-V C H VERLAG GMBHcs
dc.publisher.cityWeinheimcs
dc.relation.ispartofseries1cs
dc.relation.urihttp://onlinelibrary.wiley.com/doi/10.1002/jssc.201500845/abstractcs
dc.subjectCapillary electrophoresiscs
dc.subjectChiral separationcs
dc.subjectCyclodextrincs
dc.subjectRegioisomerscs
dc.subjectStability constantscs
dc.titleInfluence 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 baseen
dc.titleInfluence of substituent position and cavity size of the regioisomers of monocarboxymethyl-alpha-, beta-, and gamma-cyclodextrins on the apparent stability constants of their complexes with both enantiomers of Troger's basecs
local.citation.epage980-985cs
local.citation.spage980-985cs
local.identifier.publikace70
local.identifier.wok000372280600023en
local.relation.issue5cs
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