2003
DOI: 10.1002/chir.10285
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Comprehensive strategy for chiral separations using sulfated cyclodextrins in capillary electrophoresis

Abstract: This review focuses on the emerging role of sulfated cyclodextrins in the capillary electrophoretic (CE) separation of chiral analytes. Since being introduced as enantioselective agents for CE in 1995, these anionic additives have continued to demonstrate remarkable application universality. The broad spectrum of chiral compounds successfully separated using this approach includes acidic, basic, neutral, and zwitterionic species. This impressive array of analyte structures is derived from a growing diversity o… Show more

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Cited by 109 publications
(95 citation statements)
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“…The literature is dominated by CD usage, see ref. [70][71][72] for recent reviews. In many cases, CDs are combined with other PSPs to either produce or improve resolution.…”
Section: Complex-forming Selectorsmentioning
confidence: 99%
“…The literature is dominated by CD usage, see ref. [70][71][72] for recent reviews. In many cases, CDs are combined with other PSPs to either produce or improve resolution.…”
Section: Complex-forming Selectorsmentioning
confidence: 99%
“…Sulfated cyclodextrins (CDXs) are highly hydrophilic, effective chiral selectors for the separation of enantiomers of chemically diverse cationic and neutral drugs [1]. Attached to the hydroxyl sites of the macrocycle, sulfate moieties can form hydrogen and ionic bonds with guest compounds.…”
Section: Introductionmentioning
confidence: 99%
“…Therefore, chiral selectors carrying opposite charge to that of the selectands are very commonly utilized [7]. Several reviews have been published on the application of sulfated ␤-cyclodextrin (S-␤-CD) to the chiral CE [11,12].…”
Section: Introductionmentioning
confidence: 99%