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
Mono(6A-N-allylamino-6A-deoxy)perphenylcarbamoylated β-cyclodextrin: synthesis and application as a chiral stationary phase for HPLC
✍ Scribed by Xianghua Lai; Siu-Choon Ng
- Book ID
- 104253234
- Publisher
- Elsevier Science
- Year
- 2003
- Tongue
- French
- Weight
- 346 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
A novel cyclodextrin derivative: mono(6 A -N-allylamino-6 A -deoxy)perphenylcarbamoylated b-cyclodextrin was synthesized. Hydrosilylation with (EtO) 3 SiH and then reaction of the reactive siloxane with pristine silica gel afforded a facile entry into a durable, structurally well-defined chiral stationary phase capable of enantioseparation of a variety of racemic drugs.
📜 SIMILAR VOLUMES
## Abstract A novel single‐isomer positively charged β‐cyclodextrin (β‐CD), mono‐6^A^‐butylammonium‐6^A^‐deoxy‐β‐cyclodextrin tosylate (BuAM‐β‐CD), has been synthesized, characterized, and used for the enantioseparations of α‐hydroxy acids, carboxylic acids, and ampholytic analytes by capillary ele