The chemical and thermal stability of the acetamido group of (R)- and (S)-atenolol: Synthetic and chromatographic studies
- 1 January 1994
- Vol. 6 (5) , 411-419
- https://doi.org/10.1002/chir.530060509
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Stereoselective HPLC bioanalysis of atenolol enantiomers in plasma: Application to a comparative human pharmacokinetic studyChirality, 1993
- Stereoselective features of (R)‐ and (S)‐atenolol: Clinical pharmacological, pharmacokinetic, and radioligand binding studiesChirality, 1993
- Preparative resolution of the enantiomers of the β-blocking drug atenolol by chiral derivatization and high-performance liquid chromatographyJournal of Chromatography B: Biomedical Sciences and Applications, 1988
- Liquid chromatographic separation of enantiomeric alkanolamines via diastereomeric tartaric acid monoestersJournal of Chromatography A, 1984
- Ring-hydroxylated propranolol: synthesis and .beta.-receptor antagonist and vasodilating activities of the seven isomersJournal of Medicinal Chemistry, 1981
- Atenolol determination by high-performance liquid chromatography and fluorescence detectionJournal of Chromatography A, 1979
- The gas chromatographic determination of atenolol in biological samplesJournal of Pharmacy and Pharmacology, 1975
- Einige Umwandlungsprodukte des Dibenzoyl‐d‐weinsäure‐anhydridsHelvetica Chimica Acta, 1926