Area of research
Organic Chemistry · Pharmaceutical Science
Research interest
Research interests include Catalytic C–H Functionalization Methods, Asymmetric Synthesis and Catalysis, Radical Photochemical Reactions, and Sulfur-Based Synthesis Techniques.
Photoredox/Nickel-Catalyzed Hydrogenation of Alkenes Using Water as the Hydrogen Source.
Electrochemical C-H Phosphonylation of Indole with Phosphine Enabled by Chemoselective C-P Bond Cleavage.
EnT-catalysis-enabled, radical-relay cascade cyclization to access multisubstituted cyclohexane/cyclohexene.
Energy-Transfer-Mediated Radical-Relay Brook Rearrangement of Electron-Deficient Ketones.
Direct C2-arylation of indoles enabled by photoinduced XAT and Co-mediated desaturation
Photoinduced Pd-Catalyzed Formal Asymmetric Allylic Substitution of Piperidine Scaffolds
Consecutive Asymmetric Transfer Hydrogenation of C2-Acylated Quinolines and Quinoxalines: A Diastereodivergent Synthesis of Enantioenriched Tetrahydroquinolines and Tetrahydroquinoxalines Bearing <i>Endo</i>- and <i>Exo</i>cyclic Chirality.
Photosensitized Imino-Thiocyanation of Alkenes.
Wavelength-tuned, photocatalytic chemoselective hydrodefluorination
Photosensitized Imino-Thiocarbamation of Alkenes.
Photoredox Nickel-Catalyzed Coupling/Controllable Defluorination: Access to α-Fluoroarylacetic Amides and Acetates.
Nickel/Photoredox Dual-Catalyzed, Regioselective 1,2-Carboacylation of Alkenes via Synergistic Alkyl and Benzoyl Radical Coupling.
Visible-light-induced <i>meta</i>-selective sulfonylation of pyridine <i>via</i> an EDA complex.
Photoredox nickel-catalyzed radical cyclization of <i>N</i>-arylacrylamides with alkyl bromides.
MeOH-Triggered Halogen-Atom Transfer of Unactivated Alkyl Bromides Enabling the Photoredox Giese Addition.
Photoinduced, Pd-Catalyzed Enantioselective Cascade Carboamidation of Dienes to Access γ-Lactams.
C2-Benzylic C(sp<sup>3</sup>)-H Alkylation of Indoles Enabled by Photoinduced, EDA-Complex-Mediated Radical-Radical Cross-Coupling.
Regioselective Markovnikov Hydroalkylation of Unactivated Alkenes Enabled by Photoredox/Nickel Dual Catalysis.
Correction to "Pd-Catalyzed Hydrocyanation of Methylenecyclopropanes: A Highly Selective Ring-Opening Access to 2-Substituted Allylic Nitriles".
Minisci-Type Reaction Enabled by Copper-Mediated Radical-Coupling: Photocatalytic C2-Selective C-H Bis(trifluoromethyl)carbinolation of Quinolines.
Photoredox-Catalyzed Radical-Addition/Hemiaminalization Cascade of Cinnamaldehyde: Modular Access to Difluoro-5-hydroxypyrrolidinone.
Visible-Light-Induced Palladium-Mediated Allylic C-H Alkylation Reaction.
Photoredox-Driven Deoxygenative Cross-Coupling of Alcohols with Carbonyl Compounds
Photoinduced, Palladium-Catalyzed Enantioselective 1,2-Alkylsulfonylation of 1,3-Dienes
Photoredox-catalyzed hydrogenation of alkenes assisted by an <i>in situ</i> generated PPh<sub>3</sub>(OH) radical and acetic acid
Photoredox/Nickel Dual Catalysis-Enabled Aryl Formylation with 2,2-Dimethoxy-<i>N</i>,<i>N</i>-dimethylethan-1-amine as CO Source.
Amine-Borane-Mediated, Nickel/Photoredox-Catalyzed Cross-Electrophile Coupling between Alkyl and Aryl Bromides.
LncRNA CCRR maintains Ca2+ homeostasis against myocardial infarction through the FTO-SERCA2a pathway
Photosensitized 1,2-Difunctionalization of Alkenes to Access β-Amino Sulfonamides.
Iodine(III)-Mediated Trifluoroacetylation of a C(sp<sup>2</sup>)-H or C(sp)-H Bond with Masked Trifluoroacyl Reagents.