Proline–calixarene thiourea host–guest complex catalyzed enantioselective aldol reactions: from nonpolar solvents to the presence of water
Explore this paper's citation graph
- Type
- article
- Published
- 2014-03-15
- Cited by
- 16
- References
- 44
- OpenAlex
- https://openalex.org/W1989690334
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:95776437
Keywords
Thiourea, Aldol reaction, Chemistry, Cyclohexanone, Calixarene
References
- Modern aldol reactions
- New mechanistic studies on the proline-catalyzed aldol reaction.
- The Simplest "Enzyme"
- Polystyrene-supported hydroxyproline: an insoluble, recyclable organocatalyst for the asymmetric aldol reaction in water.
- Water in Stereoselective Organocatalytic Reactions
- Proline-Catalyzed Direct Asymmetric Aldol Reactions
- Organocatalytic direct asymmetric aldol reactions in water.
- Observation of Covalent Intermediates in an Enzyme Mechanism at Atomic Resolution
- Direct aldol reactions catalyzed by a heterogeneous guanidinium salt/proline system under solvent-free conditions.
- A rationally designed cocatalyst for the Morita–Baylis–Hillman reaction
- Self-assembly of an organocatalyst for the enantioselective synthesis of Michael adducts and α-aminoxy alcohols in a nonpolar medium
- Study of asymmetric aldol and Mannich reactions catalyzed by proline-thiourea host-guest complexes in nonpolar solvents
- Kinetic and stereochemical evidence for the involvement of only one proline molecule in the transition states of proline-catalyzed intra- and intermolecular aldol reactions.
- Seebach’s oxazolidinone is a good catalyst for aldol reactions
- Michael Addition of Ketones and Aldehydes to Maleimides Catalyzed by Modularly Designed Organocatalysts
- 1,3 Dipolar cycloadditions of azomethine ylides with aromatic aldehydes. syntheses of 1-oxapyrrolizidines and 1,3-oxazolidines.
- In the golden age of organocatalysis.
- The origin of enantioselectivity in aldolase antibodies: crystal structure, site-directed mutagenesis, and computational analysis.
- Self-assembly of organocatalysts for the enantioselective Michael addition of aldehydes to nitroalkenes
- Direct asymmetric aldol reactions between aldehydes and ketones catalyzed by L-tryptophan in the presence of water.
Cited by
- Confinement Effects in Catalysis Using Well-Defined Materials and Cages
- A new organocatalyst derived from abietic acid and 4-hydroxy-l-proline for direct asymmetric aldol reactions in aqueous media
- Water: the most versatile and nature’s friendly media in asymmetric organocatalyzed direct aldol reactions
- Highly stereoselective direct aldol reaction of 4-formylcoumarins with acetone catalyzed by L-proline in water–acetone mixtures
- Asymmetric Supramolecular Organocatalysis: A Complementary Upgrade to Organocatalysis
- Probing the Synergistic Catalytic Model: A Rationally Designed Urea-Tagged Proline Catalyst for the Direct Asymmetric Aldol Reaction.
- Asymmetric Michael addition reactions catalyzed by calix[4]thiourea cyclohexanediamine derivatives
- Unraveling the Role of Supramolecular Additives in a Proline-Catalyzed Reaction
- Proline—Calixarene Thiourea Host—Guest Complex Catalyzed Enantioselective Aldol Reactions: From Nonpolar Solvents to the Presence of Water.
- L-proline/cholesterol and diosgenin based thiourea cooperative system for the direct asymmetric aldol reaction in the presence of water
- Bioinspired Framework Catalysts: From Enzyme Immobilization to Biomimetic Catalysis
- Cooperative Guanidinium/Proline Organocatalytic Systems
- Asymmetric Organocatalysis in Aqueous Media
- Stereoselective organic synthesis in water: Organocatalysis by proline and its derivatives
- Zwitterionic C–N Bond Cleavage by the Accumulation of Charge: Green Synthesis of Amino Thiazolyl Benzimidazolium Bromide and Benzimidazol‐Thiazole under Microwave Irradiations
Related papers
- Asymmetric aldol reactions between cyclic ketones and benzaldehyde catalyzed by chiral Zn2+ complexes of aminoacyl 1,4,7,10-tetraazacyclododecane: effects of solvent and additives on the stereoselectivities of the aldol products
- Diastereoselective aldol reactions of cyclohexanone lithium enolate
- Gelatin Protein-Mediated Direct Aldol Reaction
- Recyclable Merrifield resin-supported thiourea organocatalysts derived from l-proline for direct asymmetric aldol reaction
- Direct asymmetric aldol reactions catalysed by trans-4-hydroxy-(S)-prolinamide in solvent-free conditions
- The 4,5-methano-l-proline as a chiral organocatalysts in direct asymmetric aldol reactions
- The pH of the reaction controls the stereoselectivity of organocatalyzed direct aldol reactions in water
- Chiral phosphine-prolineamide as an organocatalyst in direct asymmetric aldol reactions
- The boron-mediated ketone–ketone aldol reaction
- 4,4′‐Disubstituted L‐Prolines as Highly Enantioselective Catalysts for Direct Aldol Reactions