Analysis of the Mechanism of Retention on a Modified β‐Cyclodextrin/Silica Chiral Stationary Phase using a Computational Chemical Method
✍ Scribed by Tazerouti, Fairouz; Badjah‐Hadj‐Ahmed, Ahmed Yacine; Hanai, Toshihiko
- Book ID
- 127069879
- Publisher
- Taylor and Francis Group
- Year
- 2007
- Tongue
- English
- Weight
- 256 KB
- Volume
- 30
- Category
- Article
- ISSN
- 1082-6076
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📜 SIMILAR VOLUMES
Immobilized chiral stationary phases (CSP)s from mono-6 A -azido-6 A -deoxy-perphenylcarbamoylated b-cyclodextrin were prepared using an extended application of the Staudinger reaction. Their application in preparative enantioseparations of racemic mixtures was demonstrated using atropine, bendroflu
## Abstract The characteristics of the new chiral stationary phase heptakis(2,3‐di‐__O__‐methyl‐6‐__O__‐__tert__‐butyldimethylsilyl)‐β‐cyclodextrin are outlined and compared with permethyl‐ and perethyl‐β‐cyclodextrins.