Area of research
Organic Chemistry · Inorganic Chemistry
Research interest
Research interests include Chemistry, Catalysis, Aryl, Combinatorial chemistry, Amination, and Nitrene.
Harnessing the Reactivity of Nitroarene Radical Anions to Create Quinoline <i>N</i> ‐Oxides by Electrochemical Reductive Cyclization
Development and Mechanistic Study of an Iron-Catalyzed Intramolecular Nitroso Ene Reaction of Nitroarenes
Recent Advances to Mediate Reductive Processes of Nitroarenes Using Single-Electron Transfer, Organomagnesium, or Organozinc Reagents
Cu-Catalyzed Cross-Coupling of Nitroarenes with Aryl Boronic Acids to Construct Diarylamines
Rh <sub>2</sub> (II)-Catalyzed Intermolecular <i>N</i> -Aryl Aziridination of Olefins Using Nonactivated N Atom Precursors
Counterion Control of<i>t</i>‐BuO‐Mediated Single Electron Transfer to Nitrostilbenes to Construct<i>N</i>‐Hydroxyindoles or Oxindoles
Recent Advances in the Development of Catalytic Methods that Construct Medium-Ring Lactams, Partially Saturated Benzazepines and Their Derivatives
Oxidation of Nonactivated Anilines to Generate <i>N</i>-Aryl Nitrenoids
I(III)-Catalyzed Oxidative Cyclization–Migration Tandem Reactions of Unactivated Anilines
Intramolecular Pd-Catalyzed Reductive Amination of Enolizable sp<sup>3</sup>-C–H Bonds
Pd‐Catalyzed Reductive Cyclization of Nitroarenes with CO<sub>2</sub> as the CO Source
Nitroarenes as the Nitrogen Source in Intermolecular Palladium‐Catalyzed Aryl C–H Bond Aminocarbonylation Reactions
Iron-Catalyzed Reductive Cyclization of <i>o</i>-Nitrostyrenes Using Phenylsilane as the Terminal Reductant
Rh<sub>2</sub>(II)-Catalyzed Ring Expansion of Cyclobutanol-Substituted Aryl Azides To Access Medium-Sized <i>N</i>-Heterocycles
Achieving Site Selectivity in Metal-Catalyzed Electron-Rich Carbene Transfer Reactions from <i>N</i>-Tosylhydrazones
Nitroarenes as the Nitrogen Source in Intermolecular Palladium‐Catalyzed Aryl C–H Bond Aminocarbonylation Reactions
Diborane-Mediated Deoxygenation of <i>o</i>-Nitrostyrenes To Form Indoles
Control of the Chemoselectivity of Metal <i>N</i>-Aryl Nitrene Reactivity: C–H Bond Amination versus Electrocyclization
Time‐Gated Detection of Cystathionine γ‐Lyase Activity and Inhibition with a Selective, Luminogenic Hydrogen Sulfide Sensor
Promoting Reductive Tandem Reactions of Nitrostyrenes with Mo(CO)<sub>6</sub> and a Palladium Catalyst To Produce 3<i>H</i>-Indoles
Palladium‐Catalyzed Formation of <i>N</i>‐Heteroarenes from Nitroarenes using Molybdenum Hexacarbonyl as the Source of Carbon Monoxide
Mechanism of Rh<sub>2</sub>(II)-Catalyzed Indole Formation: The Catalyst Does Not Control Product Selectivity
Assembly of functionalized carbocycles or N-heterocycles through a domino electrocyclization–[1,2] migration reaction sequence
Rh<sub>2</sub>(II)-Catalyzed Ester Migration to Afford 3<i>H</i>-Indoles from Trisubstituted Styryl Azides
Copper‐Catalyzed Formation of α‐Alkoxycycloalkenones from <i>N</i>‐Tosylhydrazones
Probing the origin of carboxylate migration selectivity in Rh2(II)-catalyzed N-heterocycle formation from trisubstituted styryl azides
Development of a Suzuki Cross-Coupling Reaction between 2-Azidoarylboronic Pinacolate Esters and Vinyl Triflates To Enable the Synthesis of [2,3]-Fused Indole Heterocycles
Synthesis and Properties of Semiconducting Bispyrrolothiophenes for Organic Field‐Effect Transistors
Efficient Synthesis of 3<i>H</i>-Indoles Enabled by the Lead-Mediated α-Arylation of β-Ketoesters or γ-Lactams Using Aryl Azides
Dirhodium(II) Carboxylate Catalyzed Formation of 1,2,3‐Trisubstituted Indoles from Styryl Azides