Stereoisomer separation of flavanones and flavanone‐7‐O‐glycosides by means of nanoliquid chromatography employing derivatized β‐cyclodextrins as mobile‐phase additive

Volume: 43, Issue: 17, Pages: 3382 - 3390
Published: Aug 9, 2020
Abstract
A nanoliquid chromatographic method for the stereoisomer separation of some flavanone aglycones and 7‐ O ‐glycosides has been proposed employing a C18 capillary column and a chiral mobile‐phase additive such as cyclodextrin. The chiral separation of eriodictyol, naringenin, and hesperitin was obtained by addition of carboxymethyl‐β‐cyclodextrin to the mobile phase, whereas eriocitrin, naringin, narirutin, and hesperidin diastereoisomers were...
Paper Details
Title
Stereoisomer separation of flavanones and flavanone‐7‐O‐glycosides by means of nanoliquid chromatography employing derivatized β‐cyclodextrins as mobile‐phase additive
Published Date
Aug 9, 2020
Volume
43
Issue
17
Pages
3382 - 3390
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