1995
DOI: 10.1016/0021-9673(95)00556-5
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Separation of enantiomers of drugs by capillary electrophoresis I. γ-cyclodextrin as chiral solvating agent

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Cited by 50 publications
(20 citation statements)
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“…A systematic screening of drugs comparing a-CD [348], b-CD [349], g-CD [350] and neutral CDderivatives [341] was done by Koppenhoefer et al…”
Section: Neutral CD Derivatives a Great Variety Of Neutral Derivativmentioning
confidence: 99%
“…A systematic screening of drugs comparing a-CD [348], b-CD [349], g-CD [350] and neutral CDderivatives [341] was done by Koppenhoefer et al…”
Section: Neutral CD Derivatives a Great Variety Of Neutral Derivativmentioning
confidence: 99%
“…17 The higher concentration of 45 mmol/l ␥-CD applied in the present investigation on 86 drugs proved more successful. In fact, 13 racemates that had not been separated at the lower CSA concentration were now split into the enantiomers.…”
Section: Resultsmentioning
confidence: 85%
“…The three closely related structures (Fig. 3) allow the identification of systematic changes in the electrophoretic behaviour, dependent on the ring size of the cyclodextrin added (see Table 3; some of these data were reported previously 23,24 ). The cavity diameter is known as 5.7, 7.8, and 9.5 Å for ␣-, ␤-, and ␥-cyclodextrin, respectively.…”
Section: Resultsmentioning
confidence: 95%
“…The optical purity control was elaborated for 5,6-dihydro-2-aminotetralin [64], acetylcysteine [183], for the basic drugs denopamine, timepidium and trimetoquinol [184], for the chiral reagent 1-(9-fluorenyl)ethyl chloroformate [185] and for N-propionyl-6,7-dimethoxy-2-aminotetralin [186]. Procedures based on cyclodextrins as chiral selectors [31,187,188] were proposed for the drug screening.…”
Section: Practical Applicationsmentioning
confidence: 99%