Importance of Product Desorption in Enantioselective Hydrogenation of (E)-α-Phenylcinnamic Acid with a Cinchonidine-Modified Pd/TiO2Catalyst: Effect of Additives
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/cl/28/7/28_7_635/_pdf
Reference8 articles.
1. Enantioselective hydrogenation of α-ketoesters using cinchona modified platinum catalysts and related systems: A review
2. Enantioselective hydrogenation of (E)-α-phenylcinnamic acid on cinchonidine-modified palladium catalysts: influence of support
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1. Asymmetric transfer hydrogenation of 2,3-diphenylpropenoic acids over heterogeneous palladium catalysts modified by cinchona alkaloids;Journal of Catalysis;2024-01
2. Chiral tandem modifiers: highly efficient cinchonidine-derivative modifiers at low concentrations for the enantioselective hydrogenation of (E)-2,3-diphenylpropenoic acid over Pd/C;Catalysis Science & Technology;2022
3. Recent Advances of Pd/C-Catalyzed Reactions;Catalysts;2021-09-07
4. Effect of Methyl-substitution of the Quinoline Ring of Cinchona Alkaloids on the Performance as a Modifier for the Enantioselective Hydrogenation of (E)-2,3-di(4-methoxyphenyl)propenoic Acid Over Pd/C: Kinetic Analysis;Catalysis Letters;2020-08-09
5. Electrocatalytic asymmetric hydrogenation of α,β-unsaturated acids in a PEM reactor with cinchona-modified palladium catalysts;Electrochemistry Communications;2020-06
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