Synthesis of chiral plane-extended pyridyl alcohols for the enantioselective addition of diethylzinc to aldehydes

Authors
Kang, JYKim, HYKim, JH
Issue Date
1999-07-02
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Citation
TETRAHEDRON-ASYMMETRY, v.10, no.13, pp.2523 - 2533
Abstract
Enantiomerically pure pyridyl alcohols, 1 and 2, were prepared from readily available racemic pyridyl alcohol 3 and applied to the enantioselective addition of diethylzinc to aldehydes resulting in moderately high enantiomeric excess (90%) in the case of benzaldehyde. In this study the first example of an alteration in the configuration of the product upon change of a non-chiral and non-coordinating part of the catalyst was observed. (C) 1999 Elsevier Science Ltd. All rights reserved.
Keywords
HIGHLY DIASTEREOSELECTIVE REDUCTION; ALPHA-AMINO KETONE; ASYMMETRIC-SYNTHESIS; STEREOSPECIFIC ARYLATION; ORGANOZINC REAGENTS; AROMATIC-ALDEHYDES; CATALYSTS; BENZALDEHYDE; DIALKYLZINC; LIGANDS; HIGHLY DIASTEREOSELECTIVE REDUCTION; ALPHA-AMINO KETONE; ASYMMETRIC-SYNTHESIS; STEREOSPECIFIC ARYLATION; ORGANOZINC REAGENTS; AROMATIC-ALDEHYDES; CATALYSTS; BENZALDEHYDE; DIALKYLZINC; LIGANDS; chiral; pyridyl alcohols; enantioselective addition; diethylzinc; aldehyde
ISSN
0957-4166
URI
https://pubs.kist.re.kr/handle/201004/142054
DOI
10.1016/S0957-4166(99)00247-5
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KIST Article > Others
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