## Abstract Hydrophilic β-cyclodextrin (β-CD) and its derivatives are not soluble in organic liquids but they are highly soluble in water and can interact with enantiomers selectively to form diastereomeric complexes which enable their use as chiral selectors in chiral solvent extraction. In this p
Enantioselective extraction of terbutaline enantiomers by lipophilic tartaric acid
✍ Scribed by Tang, Ke-wen ;Zhou, Chun-shan
- Book ID
- 107506087
- Publisher
- Chinese Electronic Periodical Services
- Year
- 2003
- Tongue
- English
- Weight
- 363 KB
- Volume
- 10
- Category
- Article
- ISSN
- 1005-9784
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The lipophilic deoxyguanosine derivatives 1 are versatile molecules which, depending on to the experimental conditions, undergo different self-assembly patterns. In the presence of K ions, octamers or columnar oligomers are formed based on the G-quartet structure. In these aggregates the quartets c
Enantioselective extraction of hydrophilic 2-chloromandelic acid (CMA) enantiomers from organic to aqueous phase with hydroxypropyl-β-cyclodextrin (HP-β-CD) as the selector was investigated. Equilibrium of the extraction system was modeled using a reactive extraction model with a homogeneous aqueous