Hydrogen-bond promoted nucleophilic fluorination: concept, mechanism and applications in positron emission tomography.Inhibition of TNF-alpha, IL-1beta, and IL-6 productions and NF-kappa B activation in lipopolysaccharide-activated RAW 264.7 macrophages by catalposide, an iridoid glycoside isolated from Catalpa ovata G. Don (Bignoniaceae).Biomimetic catalytic transformation of toxic α-oxoaldehydes to high-value chiral α-hydroxythioesters using artificial glyoxalase I.Parts-per-million level loading organocatalysed enantioselective silylation of alcohols.New method of fluorination using potassium fluoride in ionic liquid: significantly enhanced reactivity of fluoride and improved selectivity.Significantly enhanced reactivities of the nucleophilic substitution reactions in ionic liquid.Imidazolium ion-terminated self-assembled monolayers on Au: effects of counteranions on surface wettability.Hydroxylation of alkyl halides with water in ionic liquid: significantly enhanced nucleophilicity of water.Dramatic enhancement of catalytic activity in an ionic liquid: highly practical Friedel-Crafts alkenylation of arenes with alkynes catalyzed by metal triflates.Hydrogenation of arenes by dual activation: reduction of substrates ranging from benzene to C60 fullerene under ambient conditions.Palladium nanoparticles supported onto ionic carbon nanotubes as robust recyclable catalysts in an ionic liquid.Organocatalytic regiospecific synthesis of 1H-indene-2-carbaldehyde derivatives: suppression of cycloolefin isomerisation by employing sterically demanding catalysts.Organocatalytic Asymmetric Synthesis of Chiral Dioxazinanes and Dioxazepanes with in Situ Generated Nitrones via a Tandem Reaction Pathway Using a Cooperative Cation Binding Catalyst.Direct Access to Chiral β-Fluoroamines with Quaternary Stereogenic Center through Cooperative Cation-Binding Catalysis.Asymmetric Aminalization via Cation-Binding Catalysis.Enantioselective Synthesis of anti-syn-Trihalides and anti-syn-anti-Tetrahalides via Asymmetric β-Elimination.Water-Enabled Catalytic Asymmetric Michael Reactions of Unreactive Nitroalkenes: One-Pot Synthesis of Chiral GABA-Analogs with All-Carbon Quaternary Stereogenic Centers.Asymmetric Synthesis of Trisubstituted Tetrahydrothiophenes via in Situ Generated Chiral Fluoride-Catalyzed Cascade Sulfa-Michael/Aldol Reaction of 1,4-Dithiane-2,5-diol and α,β-Unsaturated Ketones.Asymmetric Synthesis of α-Fluoro-β-Amino-oxindoles with Tetrasubstituted C-F Stereogenic Centers via Cooperative Cation-Binding Catalysis.Fluoride Anions in Self-Assembled Chiral Cage for the Enantioselective Protonation of Silyl Enol Ethers.DOSY NMR for monitoring self aggregation of bifunctional organocatalysts: increasing enantioselectivity with decreasing catalyst concentration.Bis-terminal hydroxy polyethers as all-purpose, multifunctional organic promoters: a mechanistic investigation and applications.Markedly enhanced recyclability of osmium catalyst in asymmetric dihydroxylation reactions by using macroporous resins bearing both residual vinyl groups and quaternary ammonium moieties.Induction of heme oxygenase-1 is involved in anti-proliferative effects of paclitaxel on rat vascular smooth muscle cells.Organocatalytic Enantioselective Cycloetherifications Using a Cooperative Cation-Binding CatalystKinetic Resolution of β-Hydroxy Carbonyl Compounds via Enantioselective Dehydration Using a Cation-Binding Catalyst: Facile Access to Enantiopure Chiral AldolsBioinspired Synthesis of Chiral 3,4-Dihydropyranones via S-to-O Acyl-Transfer ReactionsGold-catalyzed [5+2] cycloaddition of quinolinium zwitterions and allenamides as an efficient route to fused 1,4-diazepinesDirect Catalytic Asymmetric Mannich Reaction with Dithiomalonates as Excellent Mannich Donors: Organocatalytic Synthesis of (R )-SitagliptinChemoselective and repetitive intermolecular cross-acyloin condensation reactions between a variety of aromatic and aliphatic aldehydes using a robust N-heterocyclic carbene catalystOrganocatalytic Enantioselective Decarboxylative Aldol Reaction of Malonic Acid Half Thioesters with AldehydesOrganotextile CatalysisOligoethylene Glycols as Highly Efficient Mutifunctional Promoters for Nucleophilic-Substitution ReactionsSelf-association free bifunctional thiourea organocatalysts: synthesis of chiral α-amino acids via dynamic kinetic resolution of racemic azlactonesA mild and efficient method for the selective deprotection of silyl ethers using KF in the presence of tetraethylene glycolEnantioselective synthesis of α-deuterium labelled chiral α-amino acids via dynamic kinetic resolution of racemic azlactonesHydrogen bonding mediated enantioselective organocatalysis in brine: significant rate acceleration and enhanced stereoselectivity in enantioselective Michael addition reactions of 1,3-dicarbonyls to β-nitroolefinsN-Heterocyclic carbene-catalysed intermolecular Stetter reactions of acetaldehydeA Chiral-Anion Generator: Application to Catalytic Desilylative Kinetic Resolution of Silyl-Protected Secondary AlcoholsToward Understanding the Origin of Positive Effects of Ionic Liquids on Catalysis: Formation of More Reactive Catalysts and Stabilization of Reactive Intermediates and Transition States in Ionic Liquids
P50
Q38855493-B11B6F78-1891-4F0E-8A3C-04D20DCF0DE3Q40701260-155840F1-D026-4BE7-87D3-179A51A45DA0Q42292689-1B70DF01-2A2F-4CFD-898D-8FD6B7557A4CQ42580734-629F6C3A-3AF4-4C11-8197-92CF36F80DF4Q44115804-C05D906D-75ED-4F4A-AFDB-9BE0AD24A676Q44450746-91E20DA5-8E5E-4EBF-9166-E08FA5D0E450Q44726281-B3FDD360-5558-4E85-B15D-1908C122021EQ44855941-3911115D-EC17-46C2-86DB-965A29B47EE1Q45154174-021839EC-07E5-4841-8764-7DDA39D4415DQ46322124-807BD30D-AC8C-4BC3-B69A-37C0DE528C3FQ46746574-740A8189-8E53-4F44-B6C7-02BBCDBD3441Q48053149-2E9FC530-C1BE-40C5-8954-C900CF8C0210Q48168224-839FA2E6-0B91-4561-AB00-5D1CB5946980Q48178836-40C4F1AA-63C6-4DB6-9B62-FCAF376300C9Q48191139-E87D74E8-07C7-4052-867E-CDE5D5AC58ECQ48269153-C30B8573-1F14-4790-AF65-012F1079BA88Q48341867-8F22A9E1-48CD-4231-BFFB-4622363DEB4EQ52671254-56742A56-B7D2-41BD-8A9E-F82FF5DEF2ABQ53095719-7B1B2774-BE01-46AC-82CC-88CBD5AD43EDQ53108771-CFC5D6BA-FD5D-477C-A4FC-3D6CDA1F4C5CQ53464875-6521BDE5-2D7F-4BFF-83F0-11FE44A03C92Q53497345-D0DA53F5-153D-4E8D-8D7C-40FFDC42E4B4Q53619524-6ACA5BA7-808B-4A48-973A-A93D28A82E58Q53634824-87790465-E019-4754-9AF7-541EAAC11CCCQ61945830-98DD4751-0A85-49D2-B450-9FCD0CC01124Q61945834-1748716D-900A-46B5-A10D-041907D88F5FQ61945837-99FC1D83-91A9-47A5-8A81-7670D640C5C6Q61945848-F9D61361-D1B1-45EA-8C72-77292908F20CQ61945888-0745A1F9-688F-4AF2-B9F4-1BA9EF1AFCA0Q61945899-553631A4-6E01-4B30-8B51-DB15FF1959CEQ61945913-81F9AFB1-7BAE-4B90-9CB2-00387BA434FEQ61945914-718AE0FB-9161-48A0-BA16-561E05914DE5Q61945917-98A939E0-86C9-4421-8AB6-570E2CBD073DQ61945919-A5EBC337-48A1-47F4-8938-AE3AD2ED93E7Q61945923-60924F04-68D2-483C-9AF4-380967DA6DB8Q61945924-90580A69-9CFA-4DC7-A872-801FA7C6A263Q61945925-E4BEFAFA-182A-4B6A-AF01-D289E39D43BAQ61945926-AB27B622-772F-48E9-A37C-CA2A0510389BQ61945929-977F9E68-EAC5-449C-AA83-9EEA2F3C992BQ61945936-C889DA83-AAAD-44A1-A8DA-E0161F5B7BD6
P50
description
hulumtues
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researcher
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ricercatore
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scheikundige
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հետազոտող
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대한민국의 화학자
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name
Choong Eui Song
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Choong Eui Song
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Choong Eui Song
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Choong Eui Song
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Choong Eui Song
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송충의
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type
label
Choong Eui Song
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Choong Eui Song
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Choong Eui Song
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Choong Eui Song
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Choong Eui Song
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송충의
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prefLabel
Choong Eui Song
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Choong Eui Song
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Choong Eui Song
@es
Choong Eui Song
@nl
Choong Eui Song
@sl
송충의
@ko
P5034
P1153
7403253312
P21
P213
0000 0004 6089 8203
P214
209150468242104171100
P2798
P31
P496
0000-0001-9221-6789
P5034
KAC201720868
P569
1955-01-15T00:00:00Z