Interactions of non-charged tadalafil stereoisomers with cyclodextrins: Capillary electrophoresis and nuclear magnetic resonance studies
Author:
Funder
OTKA
Hungarian Academy of Sciences
Publisher
Elsevier BV
Subject
Organic Chemistry,General Medicine,Biochemistry,Analytical Chemistry
Reference29 articles.
1. Stereochemistry of the Tadalafil Diastereoisomers: A Critical Assessment of Vibrational Circular Dichroism, Electronic Circular Dichroism, and Optical Rotatory Dispersion
2. The Discovery of Tadalafil: A Novel and Highly Selective PDE5 Inhibitor. 2: 2,3,6,7,12,12a-hexahydropyrazino[1‘,2‘:1,6]pyrido[3,4-b]indole-1,4-dione Analogues
3. The identification of (−)-trans-tadalafil, tadalafil, and sildenafil in counterfeit Cialis® and the optical purity of tadalafil stereoisomers
4. Enantiomer migration order in chiral capillary electrophoresis
5. Separation selectivity in chiral capillary electrophoresis with charged selectors
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5. Comparative analysis of the full set of methylated β‐cyclodextrins as chiral selectors in capillary electrophoresis;ELECTROPHORESIS;2019-07-19
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