ASYMMETRIC-SYNTHESIS OF BETA-HYDROXY-ALPHA-AMINO ACIDS BY CONDENSATION OF ALIPHATIC AND AROMATIC-ALDEHYDES WITH ZINC(II) AND COPPER(II) COMPLEXES OF (1R)-3-HYDROXYMETHYLENE BORNAN-2-ONE GLYCINE IMINES
G. Jommi et al., ASYMMETRIC-SYNTHESIS OF BETA-HYDROXY-ALPHA-AMINO ACIDS BY CONDENSATION OF ALIPHATIC AND AROMATIC-ALDEHYDES WITH ZINC(II) AND COPPER(II) COMPLEXES OF (1R)-3-HYDROXYMETHYLENE BORNAN-2-ONE GLYCINE IMINES, Gazzetta chimica italiana, 124(7), 1994, pp. 299-300
The stereochemical outcome of the condensation reactions of aliphatic
and aromatic aldehydes with the metal complexes 1 is strongly dependen
t on the nature of the metal ion. The copper(II) complex la only affor
ds threo-P-hydroxy-cr-amino acids with fairly good enantiomeric excess
es when reacting with aromatic aldehydes. The zinc(II) complex Ib give
s a mixture of three and erythro diastereoisomers with a predominance
of the erythro forms in the case of aromatic aldehydes.