about
Selective Binding to mRNA Duplex Regions by Chemically Modified Peptide Nucleic Acids Stimulates Ribosomal Frameshifting.Macrolide Synthesis through Intramolecular Oxidative Cross-Coupling of Alkenes.Lewis Acid-Catalyzed Selective [2 + 2]-Cycloaddition and Dearomatizing Cascade Reaction of Aryl Alkynes with Acrylates.Palladium-Catalyzed Fluoroarylation of gem-Difluoroalkenes.C-F Bond Cleavage Enabled Redox-Neutral [4+1] Annulation via C-H Bond Activation.Photoredox Catalysis Induced Bisindolylation of Ethers/Alcohols via Sequential C-H and C-O Bond Cleavage.Switchable C-H Functionalization of N-Tosyl Acrylamides with Acryloylsilanes.Synthesis of Alkyl Indium Reagents by Using Unactivated Alkyl Chlorides and Their Applications in Palladium-Catalyzed Cross-Coupling Reactions with Aryl Halides.Copper-Catalyzed Dehydrogenative Diels-Alder Reaction.Palladium-Catalyzed One-Pot Highly Regioselective 6- Endo Cyclization and Alkylation of Enynoates: Synthesis of 2-Alkanone PyronesSynthesis of Polyaromatic Rings: Rh(III)-Catalyzed [5 + 1] Annulation of Enaminones with Vinyl Esters through C-H Bond FunctionalizationCombining Fluoroalkylation and Defluorination to Enable Formal [3 + 2 + 1] Heteroannulation by Using Visible-Light Photoredox OrganocatalysisBronsted Acid/Organic Photoredox Cooperative Catalysis: Easy Access to Tri- and Tetrasubstituted Alkenylphosphorus Compounds from Alcohols and P-H SpeciesRegioselective Formal [4 + 2] Cycloadditions of Enaminones with Diazocarbonyls through RhIII-Catalyzed C-H Bond FunctionalizationPalladium-Catalyzed Regioselective Olefination of O-Acetyl CyanohydrinsPalladium-Catalyzed Regiocontrollable Reductive Heck Reaction of Unactivated Aliphatic AlkenesPalladium-Catalyzed Direct Intramolecular C-N Bond Formation: Access to Multisubstituted DihydropyrrolesRegioselective Copper-Catalyzed Oxidative Coupling of α-Alkylated Styrenes with Tertiary Alkyl Radicals2H-Azirines as Potential Bifunctional Chemical Linkers of Cysteine Residues in Bioconjugate TechnologyDirect Hiyama Cross-Coupling of (Hetero)arylsilanes with C(sp2)-H Bonds Enabled by Cobalt CatalysisStereoselective C(sp2)-H Alkylation of Enamides with Unactivated Aliphatic Carboxylic Acids via Decarboxylative Cross-Coupling ReactionsDirect Substitution of Secondary and Tertiary Alcohols To Generate Sulfones under Catalyst- and Additive-Free ConditionsChromium(III)-Catalyzed Addition of Water and Alcohol to α,β-Unsaturated Ketones for the Synthesis of β-Hydroxyl and β-Alkoxyl Ketones in Aqueous MediaReactions of 5-Aminoisoxazoles with α-Diazocarbonyl Compounds: Wolff Rearrangement vs N-H InsertionPreparation of Alkyl Indium Reagents by Iodine-Catalyzed Direct Indium Insertion and Their Applications in Cross-Coupling ReactionsSynthesis of Functionalized α-Vinyl Aldehydes from EnaminonesDivergent C-H Oxidative Radical Functionalization of Olefins to Install Tertiary Alkyl Motifs Enabled by Copper CatalysisPalladium-Catalyzed Dialkylation of C-C Triple Bonds: Access to Multi-Functionalized IndenesCobalt-Catalyzed N-O and C-C Bond Cleavage in 1,2-Oxazetidines: Solvent-Controlled C-H Aminomethylation and Hydroxymethylation of HeteroarenesPalladium-Catalyzed Cascade Intramolecular Cyclization and Allylation of Enynoates with Allylic AlcoholsIron(0)-Mediated Reformatsky Reaction for the Synthesis of β-Hydroxyl Carbonyl CompoundsAlkaline-Earth Metal Catalyzed Dehydrative Allylic AlkylationRegioselective and Stereoselective Difluoromethylation of Enamides with Difluoromethyltriphenylphosphonium Bromide via Photoredox CatalysisAllylic Phosphorus Ylides Directly Generated from Alcohols with Water as the Only Byproductα-Amino Acetal: A Synthetic Intermediate for the Construction of Aza-PolycyclesIntermolecular Reductive Heck Reaction of Unactivated Aliphatic Alkenes with OrganohalidesPalladium-Catalyzed Cycloaromatization/Alkylation of o-(Alkynyl)styrenesRegioselective C-H Amidation of (Alkyl)arenes by Iron(II) CatalysisA Ba/Pd Catalytic System Enables Dehydrative Cross-Coupling and Excellent E-Selective Wittig ReactionsDivergent Protosilylation and Protoborylation of Polar Enynes
P50
Q47425280-D2C34155-80DD-4399-9D72-7E28A2717F38Q47591730-3612DBF3-57C0-4995-9799-B6EF771DFEE7Q47696261-881D658F-72A8-42A7-A818-187C086144B8Q47789680-B436471A-57C1-426D-A775-627198E5E838Q48007083-0E3B8802-BBD3-4283-9682-CC38EC04938FQ50422473-9258C818-0AC0-487C-9458-5BB5D811AC10Q50866141-305036DB-5D6B-4498-BB5A-7CC9C9887CE8Q52661359-BB297D0F-7238-4ED8-8EAE-63BB7155A46DQ54504054-07319F3F-E8DC-49BB-BEC1-680D68C488CFQ57792716-D91A4D56-BC47-4306-BBF9-B66D9C344343Q58600598-F636E81C-6AB0-4354-BBDF-92EC10F2FAE3Q88439969-FF816318-60AB-4DE5-A411-00CB5BD24380Q88749481-8E4FD7D1-2CB0-4A5E-AB29-E0B42CE03FE9Q89059226-F5A7C01C-BF00-4C70-A76A-0762799D6F1CQ89103828-EEBAFC69-2861-491C-B0FC-9D90C81DBEC9Q89168557-4FFDB1F6-11AE-4CE5-B8E7-B21462626C44Q89240086-75B01E71-DCEB-4F17-9569-5F349AAE1C36Q89253869-0C31996A-1D7C-4D2A-A231-FEAE1131F581Q89913954-806DA717-FC2D-4620-B7F9-AB05A3FC9834Q90389414-CD1A8E42-2B67-4D90-969F-18DE34DE7ECCQ90452151-4CB18C8D-73A9-44F9-A484-0E1BE7C6257BQ90937154-70EBCC9E-7D61-40F4-9EF4-575D4C3F10BFQ90957389-4C2B9B7F-7A88-4DF8-8B43-486AE792A711Q91289833-F1461D82-6DEC-495D-AEBF-C687E0043FF5Q91350802-FB3E0E39-966B-4C81-87B2-DB42A7C87C76Q91670056-27153645-1DFE-4849-AA0B-255BE91476AFQ91826629-CA4DEF90-7200-42D7-840E-80E5B5F8B157Q91877311-6DF5C866-2DB6-48E1-A504-7AA7A8161D2EQ91929775-1FFEBBA8-637E-418E-A437-EF658526D917Q91970470-0D659E4D-9EFA-41CF-9086-2D14D8F8FDF1Q91984986-C36407DA-65D2-4079-8A4D-8893D48E23BBQ92002844-A2B4D01A-93D4-4BA1-BFB8-5BA75BD9D897Q92146140-4DC06F2D-02C1-4777-A853-BFB2FE40BAE5Q92335116-A5730705-BAF0-483D-B4A7-C546274AEC7DQ92338388-BD1B39AB-A48E-47C9-9883-FBFF31AE8E88Q92493581-0D7E8E65-FE13-47B0-831B-A050993CC22FQ92634202-1B3AB5C1-4004-4206-8960-27CC62024EC1Q92672998-C0AEDE22-7B89-45A5-A3F4-DA0477BF9DC3Q92726052-67F05573-6E8C-45CD-84C7-FF7A50901E4AQ92786210-59B2C64D-366C-4B6A-84C2-E69537B28D8B
P50
description
researcher
@en
wetenschapper
@nl
name
Teck-Peng Loh
@en
Teck-Peng Loh
@nl
type
label
Teck-Peng Loh
@en
Teck-Peng Loh
@nl
prefLabel
Teck-Peng Loh
@en
Teck-Peng Loh
@nl
P31
P496
0000-0002-2936-337X