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Ann Pharm Fr ; 54(3): 103-8, 1996.
Article in French | MEDLINE | ID: mdl-8794578

ABSTRACT

The study of the kinetic of cyclisation reaction of the additional compound of the mercaptoacetic ethylester on a benzylideneacetophenone was proposed. With the chromatography a retro-Michael reaction was obtained. The H NMR alone permitted to show the order 1 for the kinetic of cyclization and according to the amine used like reaction catalyst, two diastereoisomers could be formed.


Subject(s)
Chalcone/pharmacokinetics , Thioglycolates/pharmacokinetics , Chalcone/administration & dosage , Chromatography, High Pressure Liquid , Cyclization , Drug Combinations , In Vitro Techniques , Magnetic Resonance Spectroscopy , Mass Spectrometry , Stereoisomerism , Thioglycolates/administration & dosage
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