HPLC and 1H-NMR study of chiral recognition in some thromboxane antagonists induced by β-cyclodextrin-Reference-Cited by-同舟云学术

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HPLC and 1H-NMR study of chiral recognition in some thromboxane antagonists induced by β-cyclodextrin

Published:1991-01 Issue:10-12 Volume:9 Page:787-792
ISSN:0731-7085
Container-title:Journal of Pharmaceutical and Biomedical Analysis
language:en
Short-container-title:Journal of Pharmaceutical and Biomedical Analysis

Author:

Casy A.F.,Cooper A.D.,Jefferies T.M.,Gaskell R.M.,Greatbanks D.,Pickford R.

Publisher

Elsevier BV

Subject

Clinical Biochemistry,Spectroscopy,Drug Discovery,Pharmaceutical Science,Analytical Chemistry

Reference25 articles.

1. Resolution of some chiral mandelic acid derivatives into enantiomers by reversed-phase high-performance liquid chromatography via α- and β-cyclodextrin inclusion complexes

2. Separation of Drug Stereoisomers by the Formation of β-Cyclodextrin Inclusion Complexes

3. On-line recovery of trimeprazine enantiomers following chiral separation by reversed-phase high-performance liquid chromatography using a β-cyclodextrin-containing mobile phase

4. Displacement chromatography on cyclodextrin—silicas

5. Cyclodextrins as chiral nuclear magnetic resonance shift reagents

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1. Characterization of group-inclusion complexations of rhodamine derivatives with native and 2,6-di-O-methylated β-cyclodextrins;Journal of Inclusion Phenomena and Macrocyclic Chemistry;2020-01-24

2. The application of absolute quantitative1H NMR spectroscopy in drug discovery and development;Expert Opinion on Drug Discovery;2016-06-03

3. Water soluble biocompatible vesicles based on polysaccharides and oligosaccharides inclusion complexes for carotenoid delivery;Carbohydrate Polymers;2015-09

4. Chiral discrimination of sibutramine enantiomers by capillary electrophoresis and proton nuclear magnetic resonance spectroscopy;Archives of Pharmacal Research;2012-04

5. Determination of the Isomeric Composition of Drugs;NMR Spectroscopy in Drug Development and Analysis;2007-12-10

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