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

Citation
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
Citations number
14
Categorie Soggetti
Chemistry
Journal title
ISSN journal
00165603
Volume
124
Issue
7
Year of publication
1994
Pages
299 - 300
Database
ISI
SICI code
0016-5603(1994)124:7<299:AOBABC>2.0.ZU;2-G
Abstract
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.