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Arzneimittelforschung ; 36(8): 1157-61, 1986 Aug.
Article in German | MEDLINE | ID: mdl-2946303

ABSTRACT

The absolute configuration of (+)-celiprolol ([alpha]D = +6.3 degrees in CHCl3) was established by a 9-step synthesis via the (+) (R)-acetonide of (R)-glyceraldehyde. This result was confirmed by the Cupra-A CD-spectra of the isopropyl and hydroxy analogs. The enantiomeric purity was determined by NMR analysis of the diastereomeric amide esters obtained by reaction of celiprolol with 2 mol of alpha-methoxy-alpha-trifluoromethyl-phenylacetic acid chloride (Mosher's reagent).


Subject(s)
Propanolamines/analysis , Celiprolol , Circular Dichroism , Magnetic Resonance Spectroscopy , Molecular Conformation , Propanolamines/isolation & purification , Stereoisomerism
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