Abstract: The process described makes it possible to obtain optically pure 4-amino-3-hydroxycarboxylic acids by means of a series of stereoselective steps. The starting material is an alpha-amino acid in the L or D configuration, with which Meldrum's acid is reacted. The resulting pyrrolone derivative is reduced prior to opening of the pyrrolidine ring. The invention also relates to the new products obtained by the said process and to the pyrrolone derivatives obtained as intermediates.
Type:
Grant
Filed:
July 2, 1986
Date of Patent:
December 18, 1990
Assignee:
Sanofi, S.A. and Institut National de la Sante et de la Recherche Medicale
Inventors:
Patrick Jouin, Dino Nisato, Bertrand Castro