Direct covalent immobilizaion of chiral phosphine oxide: Hollow mesoporous polystyrene nanospheres as a platform for efficient heterogeneous enantioselective reductive aldol reaction
Author:
Funder
National Natural Science Foundation of China
Publisher
Elsevier BV
Subject
Physical and Theoretical Chemistry,Process Chemistry and Technology,Catalysis
Reference42 articles.
1. 3,3′-Bithiophene- based chiral bisphosphine oxides as organocatalysts in silicon-derived Lewis acid mediated reactions;Rossi;Synlett,2020
2. Recent advances in asymmetric phosphine oxide catalysis;Kotani;Tetrahedron Lett.,2020
3. Phosphine oxide-catalyzed asymmetric aldol reactions and double aldol reactions;Kotani;Chem. Pharm. Bull.,2019
4. Enantioselective reactions catalyzed by phosphine oxides;Ayad;Tetrahedron,2019
5. Chiral phosphine oxides in present-day organocatalysis;Benaglia;Org. Biomol. Chem.,2010
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2. Heterogeneous organo/metal cooperative catalysis: One-pot immobilization of Pd(PPh3)4 and chiral phosphoric acid to hollow mesoporous polystyrene nanospheres for efficient asymmetric α-allylation of aldehydes;Applied Catalysis A: General;2024-08
3. Pore size-dependent confinement: High selectivity promoted by pore-confined Au single-atom catalysts in direct arylation;Applied Catalysis A: General;2024-04
4. Homogeneous-like photocatalysis: covalent immobilization of an iridium(III) complex onto polystyrene brushes grafted on SiO2 nanoparticles as a mass/charge transfer-enhanced platform;Dalton Transactions;2024
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