1.
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.