Catalysis by amino acid-derived tetracoordinate complexes: Enantioselective addition of dialkylzincs to aliphatic and aromatic aldehydes

Citation
Bd. Dangel et R. Polt, Catalysis by amino acid-derived tetracoordinate complexes: Enantioselective addition of dialkylzincs to aliphatic and aromatic aldehydes, ORG LETT, 2(19), 2000, pp. 3003-3006
Citations number
58
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
ORGANIC LETTERS
ISSN journal
15237060 → ACNP
Volume
2
Issue
19
Year of publication
2000
Pages
3003 - 3006
Database
ISI
SICI code
1523-7060(20000921)2:19<3003:CBAATC>2.0.ZU;2-6
Abstract
GRAPHICS Me2Zn and Et2Zn added to aromatic and aliphatic aldehydes in the presence o f 3 mol % of 2. (S)-1-Phenylethanol (91% ee) and (S)-1-phenylpropanol (86% ee) were synthesized from benzaldehyde and (S)-1-furan-2-yl-1-propanol (86% ee) from 2-furaldehyde. Nonanal and 3-phenylpropanal provided (S)-3-undeca nol (96% ee) and (S)-1-phenyl-3-pentanol (94% ee). A solid-phase variant wa s effective with reduced ee's (e.g,, 86% ee -> 79% ee) for (S)-1-phenylprop anol.