Chiral Separation of Acebutolol by Derivatization and High-Performance Liquid Chromatography
Author:
Publisher
Informa UK Limited
Subject
Molecular Medicine
Link
http://www.tandfonline.com/doi/pdf/10.1080/10826079508010454
Reference11 articles.
1. Determination of metoprolol enantiomers in plasma and urine using (S)-(−)-phenylethyl isocyanate as a chiral reagent
2. Stereoselective clearance and distribution of intravenous propranolol
3. Stereoselective binding of propranolol to human plasma, α1-acid glycoprotein, and albumin
4. Plasma levels of (+) and (−)−propranolol and 4-hydroxypropranolol after administration of racemic (+/-)-propranolol in man.
5. Preparative resolution of the enantiomers of the β-blocking drug atenolol by chiral derivatization and high-performance liquid chromatography
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1. Spectrofluorimetric Determination of Drugs Containing Active Methylene Group Using N1-Methyl Nicotinamide Chloride as a Fluorigenic Agent;Chemical and Pharmaceutical Bulletin;2006
2. Determination of Methanol by 4-[N-Methyl,N-(1-naphthylmethyl)]-amino-4-oxo-butanoic Acid in Presence of 4-Dimethylaminopyridine and 1-Ethyl-3-(3-dimethylaminopropyl) Carbodiimide Hydrochloride as Catalysts;Analytical Letters;2003-01-05
3. Liquid chromatographic enantioseparation of β-blocking agents with (1R,2R)-1,3-diacetoxy-1-(4-nitrophenyl)-2-propyl isothiocyanate as chiral derivatizing agent;Journal of Chromatography A;2001-03
4. First derivative spectrophotometric, TLC-densitometric, and HPLC determination of acebutolol HCL in presence of its acid-induced degradation product;Journal of Pharmaceutical and Biomedical Analysis;2001-02
5. Recent chromatographic and electrophoretic enantioseparations of cardiovascular drugs;Biomedical Chromatography;1999-05
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