Aqueous asymmetric aldol reaction catalyzed by nanomagnetic solid acid SO42−/Zr(OH)4–Fe3O4
Author:
Publisher
Elsevier BV
Subject
Metals and Alloys,Mechanical Engineering,Mechanics of Materials
Reference32 articles.
1. The Vinylogous Aldol and Related Addition Reactions: Ten Years of Progress
2. Catalytic Enantioselective Aldol Additions to Ketones
3. Total Syntheses of Carbohydrates: Organocatalyzed Aldol Additions of Dihydroxyacetone
4. Current progress in the asymmetric aldol addition reaction
5. Carbon-Based Solid Acid as an Efficient and Reusable Catalyst for Cross-Aldol Condensation of Ketones with Aromatic Aldehydes under Solvent-Free Conditions
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1. S/CuMgAl-41 as an efficient Hybrid catalyst for asymmetric addition reaction in isopropyl alcohol solvent;Molecular Catalysis;2024-03
2. Development of SO42−/ZnAl2O4–ZrO2 composite solid acids for efficient synthesis of green biofuels via the typical esterification reaction of oleic acid with methanol;Reaction Kinetics, Mechanisms and Catalysis;2023-07-03
3. Caesium carbonate functionalized magnetic nanoparticles: An efficient heterogeneous and reusable inorganic catalyst for aldol reaction in water;Inorganic Chemistry Communications;2023-03
4. Sulfonation of pyrene-based metal–organic framework for the encapsulation of chiral organocatalyst and application in asymmetric aldol addition;Applied Catalysis A: General;2023-01
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