Highly enantioselective Henry reaction catalyzed by chiral tridentate heteroorganic ligands

Tetrahedron Asymmetry

Volumn 20, Issue 13, 2009, Pages 1547-1549

  Rachwalski, Michał ^a,b   Leśniak, Stanisław ^b   Sznajder, Ewelina ^b   Kiełbasiński, Piotr ^a  

^a CENTRE OF MOLECULAR AND MACROMOLECULAR STUDIES   (Poland)

^b UNIVERSITY OF LODZ   (Poland)

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE; AMINE; AMINO ACID; CARBON; COPPER ACETATE; HYDROXYL GROUP; SULFUR;

ADDITION REACTION; ALDOL REACTION; ARTICLE; CATALYST; ENANTIOMER; ENANTIOSELECTIVITY; PRIORITY JOURNAL; STEREOCHEMISTRY;

EID: 67651095998     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2009.06.015     Document Type: Article

References (15)

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13. 10 ligands 3d-f turned out to be efficient catalysts for the diethylzinc addition to benzaldehyde; for their synthesis and application see Leśniak, S.; Rachwalski, M.; Sznajder, E.; Kiełbasiński, P., submitted for publication.
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15. Ferrocenyl(hydroxymethyl)aziridines were recently found to be good catalysts for the Henry reaction. However, instead of copper acetate, diethylzinc was used as the metal component: see Ref. 6.