Synthesis of chiral plane-extended pyridyl alcohols for the enantioselective addition of diethylzinc to aldehydes
- Authors
- Kang, JY; Kim, HY; Kim, 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
- Appears in Collections:
- KIST Article > Others
- Files in This Item:
There are no files associated with this item.
- Export
- RIS (EndNote)
- XLS (Excel)
- XML
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.