The Influence of the Substituent Position in Monocarboxymethyl-gamma-cyclodextrins on Enantioselectivity in Capillary Electrophoresis

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dc.contributor.authorŘezanka Michalcs
dc.contributor.authorŘezanka Pavelcs
dc.contributor.authorRokosová Lenkacs
dc.contributor.authorŘezanková Kláracs
dc.contributor.authorBláhová Markétacs
dc.contributor.authorSýkora Davidcs
dc.contributor.authorJindřich Jindřichcs
dc.contributor.authorKrál Vladimírcs
dc.date.accessioned2018-09-25T11:44:30Z
dc.date.available2018-09-25T11:44:30Z
dc.date.issued2014cs
dc.format.extent6cs
dc.identifier.issn1615-9306cs
dc.identifier.urihttps://dspace.tul.cz/handle/15240/26796
dc.language.isoengcs
dc.publisherWILEY-VCH Verlag GmbH & Co. KGaA, Weinheimcs
dc.publisher.cityWeinheimcs
dc.relation.ispartofseries1cs
dc.subjectCapillary electrophoresiscs
dc.subjectChiral separationcs
dc.subjectEnantioselectivitycs
dc.subjectRegioisomerscs
dc.subjectSubstituted cyclodextrinscs
dc.titleThe Influence of the Substituent Position in Monocarboxymethyl-gamma-cyclodextrins on Enantioselectivity in Capillary Electrophoresiscs
local.citation.epage2779-2784cs
local.citation.spage2779-2784cs
local.identifier.publikace80
local.identifier.wok000342909300020en
local.relation.issue19cs
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