Monte Carlo simulations of the chiral recognition of fenoprofen enantiomers by cyclomaltoheptaose (β-cyclodextrin)
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference15 articles.
1. Separation of Drug Stereoisomers by the Formation of β-Cyclodextrin Inclusion Complexes
2. Fenoprofen
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4. Chiral discrimination of the analgesic cizolirtine by using cyclodextrins: A1H NMR study on the solution structures of their host-guest complexes
5. Molecular modelling of the inclusion complexes between β-cyclodextrin and (R)/(S)-methylphenobarbitone and its application to HPLC
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1. Chapter 10: Molecular Simulation of Chiral Selector‒Enantiomer Interactions throughDocking: Antimalarial Drugs as Case Study;Capillary Electrophoresis;2017-08-07
2. Enantioselective extraction of clorprenaline enantiomers with hydrophilic selector of sulfobutylether-β-cyclodextrin by experiment and modeling;Journal of Central South University;2014-03
3. An expanded cellular automata model for enantiomer separations using a β-cyclodextrin stationary phase;Journal of Chromatography A;2013-05
4. Simulations of docking C60 in β-Cyclodextrin;Journal of Molecular Liquids;2011-08
5. Extended Surface Chirality for Enantiospecific Adsorption;Chemistry - A European Journal;2008-09-19
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