Enantiomer-differentiating hydrogenation of methyl 3-cyclopropyl-2-methyl-3-oxopropanoate over tartaric acid-modified nickel
Author:
Publisher
Elsevier BV
Subject
Physical and Theoretical Chemistry,Process Chemistry and Technology,Catalysis
Reference23 articles.
1. Stereoselective Organic Synthesis via Dynamic Kinetic Resolution
2. Asymmetric hydrogenation of .beta.-keto carboxylic esters. A practical, purely chemical access to .beta.-hydroxy esters in high enantiomeric purity
3. YEAST REDUCTION OF ETHYL ACETOACETATE: (S)-( + )-ETHYL 3-HYDROXYBUTANOATE
4. Highly Enantioselective Hydrogenation of .beta.-Keto Esters under Mild Conditions
5. Diastereo- and enantio-selective reduction of 2-methyl-3-oxobutanoate by bakers' yeast
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1. Structure-selectivity relationship in the cleavage of spirocyclopropyl oxindoles: An experimental and theoretical investigation;Journal of Molecular Structure;2017-10
2. Dynamic Kinetic Resolution (DKR);Separation of Enantiomers;2014-05-02
3. 8.04 Reduction of CO to CHOH by Metal-Catalyzed Hydrogenation and Transfer Hydrogenation;Comprehensive Organic Synthesis II;2014
4. Catalysis with Chirally Modified Metal Surfaces: Scope and Mechanisms;Catalytic Methods in Asymmetric Synthesis;2011-07-07
5. Chiral Catalysts;Chirality from Dynamic Kinetic Resolution;2011-04-04
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