1990
DOI: 10.1016/s0021-9673(01)89435-8
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(S)-2-Hydroxyprophyl-β-cyclodextrin, a new chiral stationary phase for reversed-phase liquid chromatography

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Cited by 150 publications
(49 citation statements)
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“…Hence, a great number of compounds which are unresolved or partially resolved on native ␤-cyclodextrin can be separated on the ␤-RSP. 32,33 Capillary electrophoresis carried out in our laboratory with several cyclodextrins (native and derivatized) confirmed the ability of this selector to resolve Mtd enantiomers. 34 As indicated in Table 3, efficiency and resolution decrease rapidly as a function of the flow rate (in the range 0.4-1 ml/min).…”
Section: Cyclobond I 2000 Rspmentioning
confidence: 63%
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“…Hence, a great number of compounds which are unresolved or partially resolved on native ␤-cyclodextrin can be separated on the ␤-RSP. 32,33 Capillary electrophoresis carried out in our laboratory with several cyclodextrins (native and derivatized) confirmed the ability of this selector to resolve Mtd enantiomers. 34 As indicated in Table 3, efficiency and resolution decrease rapidly as a function of the flow rate (in the range 0.4-1 ml/min).…”
Section: Cyclobond I 2000 Rspmentioning
confidence: 63%
“…30 Furthermore, secondary interactions with the hydroxypropyl group can drastically enhance chiral recognition versus the native cyclodextrin. 31,32 Finally, hydroxypropyl groups are flexible, allowing better hydrogen bonding with analytes. Hence, a great number of compounds which are unresolved or partially resolved on native ␤-cyclodextrin can be separated on the ␤-RSP.…”
Section: Cyclobond I 2000 Rspmentioning
confidence: 99%
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“…In HP-β-CD, some hydroxyl groups are substituted with hydroxypropyl functional groups. This modification allows for a more stereospecific and stronger interaction between the hydroxyl groups and hydrogen-bonding moiety present in the drug structure [27]. Cyclodextrins are well suited to chromatography since the inclusion process is stereoselective and reversible.…”
Section: Resultsmentioning
confidence: 99%
“…Besides the native cyclodextrin, functionalized cyclodextrins, such as hydroxypropyl-β-CD, 11,16 naphthylethylcarbamoylated-β-CD, 17 perphenylcarbamoylated β-CD, 9 sulfated CDs 18 etc., were also be used as chiral selectors to expand the range of compounds that are enantioresolvable. Among functionalized CDs, sulfated CDs are recognized as being the best effective selectors, especially when they were used in CE as chiral additives.…”
Section: Introductionmentioning
confidence: 99%