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Enantioselective separations by capillary GC on derivatized cyclodextrins. Part 2: Determination of enantiomeric excess of some racemic 2,3-isopropylidene-1,2,3-cyclohexanetriol derivatives on permethyl α-, β-, and γ-cyclodextrins

✍ Scribed by Jaques, K. ;Buda, W. ;Dumortier, L. ;Van der Eycken, J. ;Venema, Arnold ;Sandra, Pat


Publisher
John Wiley and Sons
Year
1994
Tongue
English
Weight
167 KB
Volume
17
Category
Article
ISSN
0935-6304

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✦ Synopsis


Abstract

Capillary GC on permethyl α‐, β‐, and γ‐cyclodextrins has been applied to separate and quantify the enantiomers of some 2,3‐iso‐propylidene‐1,2,3‐cyclohexanetriol derivatives. Quantitative CGC data are compared to those obtained with chiral shift ^1^H NMR.


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Enantioselective separations by capillar
✍ Jaques, K. ;Buda, W. M. ;Pottie, M. ;Van der Eycken, J. ;Vandewalle, M. ;Venema, 📂 Article 📅 1993 🏛 John Wiley and Sons 🌐 English ⚖ 337 KB 👁 1 views

## Abstract The enantioseparation of some 2,2‐dialkyl‐4‐alkoxycarbonyl‐1,3‐dioxolane derivatives, which are important intermediates in the total synthesis of a number of biologically active compounds, was studied by means of capillary gas chromatography (CGC). The chromatographic results, obtained

Enantioselective separations by capillar
✍ K. Jaques; W. M. Buda; Prof. Dr. A. Venema; P. Sandra 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 English ⚖ 480 KB

## Abstract An evaluation of the effects of differently derivatized cyclodextrins and analyte geometry for a series of 2,2‐dialkyl‐4‐alkoxycarbonyl‐1,3‐dioxolane derivatives on enantioselectivity has been performed. It was shown that changes in the cyclodextrin cavity size, caused by either the cho