Ruthenium-Catalysed Efficient Asymmetric Transfer Hydrogenation of Aromatic Ketones using Cinchona Alkaloids as Chiral Ligands
Author:
Affiliation:
1. Key Laboratory of Catalysis Science and Technology of Chongqing Education Commission, Chongqing Key Laboratory of Catalysis and Functional Organic Molecules, Chongqing Technology and Business University, Chongqing 400067, P.R. China
Publisher
SAGE Publications
Subject
General Chemistry
Link
http://journals.sagepub.com/doi/pdf/10.3184/174751913X13845949778485
Reference18 articles.
1. Asymmetric Synthesis of Active Pharmaceutical Ingredients
2. Synthesis and Catalytic Activities of (S)-1-formylpyrrolidine-2-carboxylic Acid Derivatives for the Enantioselective Reductions of Both a Ketone and a Ketimine
3. Ruthenium(II)-Catalyzed Asymmetric Transfer Hydrogenation of Ketones Using a Formic Acid−Triethylamine Mixture
4. Asymmetric homogeneous hydrogenations at scale
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1. In situ hydrodeoxygenation of vanillin over Ni–Co–P/HAP with formic acid as a hydrogen source;RSC Advances;2021
2. Catalytic asymmetric transfer hydrogenation of ketones: recent advances;Tetrahedron: Asymmetry;2015-08
3. Asymmetric Hydrogenation of Aromatic Ketones Catalysed by L-Proline Derivatives Modified Ru/γ-Al2O3;Journal of Chemical Research;2014-07
4. ChemInform Abstract: Ruthenium-Catalyzed Efficient Asymmetric Transfer Hydrogenation of Aromatic Ketones Using Cinchona Alkaloids as Chiral Ligands.;ChemInform;2014-06-02
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