JOURNAL ARTICLE

Lithium Binaphtholate Catalyzed Direct Asymmetric Aldol-Tishchenko Reaction

Patrick Brady Contributor Hisashi YamamotoM. Nakajima

Year: 2011 Journal:   Synfacts Vol: 2011 (07)Pages: 0742-0742   Publisher: Georg Thieme Verlag

Abstract

The direct aldol-Tishchenko reaction of ketones with aldehydes catalyzed by a chiral lithium binaphtholate is described. Initially, a mixture of monobenzoyl 1,3-diols is formed. Subsequent hydrolysis generates the 1,3-diols as single diastereomers and in high yield and enantiomeric excess. The catalyst is inexpensive and can be easily prepared.

Keywords:
Chemistry Aldol reaction Diastereomer Catalysis Yield (engineering) Lithium (medication) Hydrolysis Enantiomeric excess Organic chemistry Enantiomer Enantioselective synthesis

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Topics

Analytical Chemistry and Chromatography
Physical Sciences →  Chemistry →  Spectroscopy
Asymmetric Synthesis and Catalysis
Physical Sciences →  Chemistry →  Organic Chemistry
Asymmetric Hydrogenation and Catalysis
Physical Sciences →  Chemistry →  Inorganic Chemistry

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