Relative retention b, The capacity facJor of the more retained enantiomer
Cyclodextrins as chiral stationary phases in capillary gas chromatography I. Pentylated α-cyclodextrin
✍ Scribed by Wilfried A. König; Sabine Lutz; Petra Mischnick-Lübbecke; Bärbel Brassat; Gerhard Wenz
- Publisher
- Elsevier Science
- Year
- 1988
- Tongue
- English
- Weight
- 351 KB
- Volume
- 447
- Category
- Article
- ISSN
- 1873-3778
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📜 SIMILAR VOLUMES
The properties of hexa kis(3-0-acetyl-2,6-di-O-pentyl)-a-cyclodextrin as a chiral stationary phase for capillary gas chromatography are described. For the first time the enantiomers of a series of different lactones are separated and their order of elution is assigned. Moreover, the enantiomers of t
Perpentylated y-cyclodextrin is a very hydrophobic liquid which exhibits enantioselectivity toward a number of non-polar chiral substrates including the saturated hydrocarbons cisand transpinane, P-chiral olefins, iron(0) tricarbonyl complexes of prochiral olefins and 3,3,8,8-tetramethyl-trans-cyclo
## Abstract The following carbamate derivatives of cyclodextrins (CDs) were prepared as novel chiral stationary phases for capillary gas chromatography: hexakis(2,6‐di‐__O__‐pentyl)‐α‐cyclodextrin hexa(3‐__n__‐propyl, 3‐isopropyl, and 3‐phenylcarbamate), heptakis‐(2,6‐di‐__O__‐pentyl)‐β‐cyclodextri