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Blockers of β-Adrenergic Receptors – a Group of Chiral Agents Stereoselective Synthesis of β-Blockers


Authors: R. Čižmáriková;  J. Valentová;  A. J. Hutt 1;  S. Sedláková
Authors‘ workplace: Farmaceutická fakulta Univerzity Komenského v Bratislave, Katedra chemickej teórie liečiv, SR ;  Department of Pharmacy, King’s College London, University of London, UK 1
Published in: Čes. slov. Farm., 2005; 54, 201-206
Category: Review Articles

Overview

Besides chromatographic methods and biocatalyzed reactions, another alternative method of obtaining enantiomeric forms of ß-blockers is stereoselective synthesis. This paper links up with two preceding surveys concerning ß-blockers – groups of chiral agents and presents a survey of the hitherto published enantioselective syntheses of (R)- and (S)-enantiomers of β-blockers. In the group of arylaminoethanols, mainly selective reduction of prochiral ketones in the presence of metallic complexes is used in this type of synthesis. Enantiomerically pure ß-blockers of the aryloxyaminopropanol type are synthesized by means of a reaction of pertinent phenols with different chiral precursors, such as (R) and (S)-chloromethyloxirans, (S)-glycidoltosylate, (S)- or (R)-2,3-O-isopropylideneglyceroltosylate, E-(2S,3S)-3-trimethylsilylglycidol and (S)-3-terc-butyl-5- -phenyl-oxazolidine-5-ylmethanol. Many of these chiral semiproducts can be prepared from natural substances, such as D-mannitol and L-ascorbic acid.

Key words:
ß-blockers – stereoselective synthesis – arylaminoethanols – aryloxyaminopropanols – enantioselective reduction – chiral precursors


Labels
Pharmacy Clinical pharmacology
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