Determination of the Configuration of Diastereoisomers of 2-Alkyl-3-hydroxybutanoates with Gas Chromatography
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/63/1/63_1_298/_pdf
Reference5 articles.
1. An introduction of chiral centers into acyclic systems based on stereoselective ketone reduction
2. Chemistry of carbanions. XXIII. Use of metal complexes to control the aldol condensation
3. 2-methylacetoacetate reductase and possible propionyl coenzyme A condensing enzyme activity in branched chain volatile fatty acid synthesis by Ascaris lumbricoides.
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1. Stereochemical Control in Microbial Reduction. XXIX. Mechanism of Stereochemical Control with an Additive in the Diastereoselective Reduction byGeotrichum candidum;Bulletin of the Chemical Society of Japan;1997-07
2. Stereochemical Control in Microbial Reduction. XXV. Additives Controlling Diastereoselectivity in a Microbial Reduction of Ethyl 2-Methyl-3-oxobutanoate;Bulletin of the Chemical Society of Japan;1995-01
3. Stereochemical Control in Microbial Reduction. XXIII. Thermal Treatment of Bakers’ Yeast for Controlling the Stereoselectivity of Reductions;Bulletin of the Chemical Society of Japan;1994-08
4. A kinetic study and application of a novel carbonyl reductase isolated from rhodococcus erythropolis;Bioorganic & Medicinal Chemistry;1994-06
5. Stereoselective synthesis of ethyl (2S,3S)-anti-2-methyl-3-hydroxybutanoate mediated by an Oxidoreductase from Geotrichum candidum;Tetrahedron Letters;1994-01
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