Area of research
Organic Chemistry
Research interest
Research interests include Chemistry, Catalysis, Aryl, Decarboxylation, Electrochemistry, and Halogenation.
Amine-Controlled, Transition-Metal-Catalyzed Hydrodefluorination and Defluoroamination of Fluoroarenes with 8-Aminoquinoline as a Directing Group
Electrochemical strategies for NaX-mediated hydrolysis and alcoholysis of hydrosilanes under mild conditions
Explore the toxicological mechanism of 6PPD-Q on human health through a novel perspective: The interaction between lactate dehydrogenase and 6PPD-Q
Electrooxidative Ni‐Catalyzed Decarboxylation of Arylacetic Acids Towards the Synthesis of Carbonyls under Air Conditions
Visible-light-induced C(sp<sup>3</sup>)–C(sp<sup>3</sup>) bond formation<i>via</i>radical/radical cross-coupling
Nickel-catalyzed reductive coupling of nitroarenes and phosphine oxides to access phosphinic amides
An Electrochemical Method for Deborylative Hydroxylation of Arylboronic Acids under Metal‐free Conditions
Nickel-Catalyzed 1,1-Dihydrophosphinylation of Nitriles with Phosphine Oxides
Bromide ion promoted practical synthesis of phosphinothioates of sulfinic acid derivatives and H-phosphine oxides
Electrochemical Synthesis of Aryl Sulfonates from Sodium Sulfinates and Phenols under Metal-Free Conditions
An electrochemical method for deborylative selenylation of arylboronic acids under metal- and oxidant-free conditions
Electrochemical strategies for <i>N</i>-cyanation of secondary amines and α <i>C</i>-cyanation of tertiary amines under transition metal-free conditions
An electrochemical method for deborylative seleno/thiocyanation of arylboronic acids under catalyst- and oxidant-free conditions
Transition metal-free electrocatalytic halodeborylation of arylboronic acids with metal halides MX (X = I, Br) to synthesize aryl halides
Environmentally sustainable production and application of acyl phosphates
Selective C–C bond cleavage of amides fused to 8-aminoquinoline controlled by a catalyst and an oxidant
Conversions of aryl carboxylic acids into aryl nitriles using multiple types of Cu-mediated decarboxylative cyanation under aerobic conditions
Dichloromethane as a methylene synthon for regioselective linkage of diverse carboxylic acids: Direct access to methylene diesters under metal-free conditions
Pd-Catalyzed Decarboxylative <i>Ortho</i>-Halogenation of Aryl Carboxylic Acids with Sodium Halide NaX Using Carboxyl as a Traceless Directing Group
Facile synthesis of methylthiomethyl esters through Pummerer-type rearrangement of carboxylic acids and DMSO under metal-free conditions
Cu-catalyzed decarboxylative iodination of aryl carboxylic acids with NaI: A practical entry to aryl iodides under aerobic conditions
Inexpensive NaX (X = I, Br, Cl) as a halogen donor in the practical Ag/Cu-mediated decarboxylative halogenation of aryl carboxylic acids under aerobic conditions
Nucleophile-controlled mono- and bis-phosphonation of amino-2-en-1-ones <i>via</i> catalyst-free C(sp<sup>3</sup>)–N bond cleavage
Reversible solid-state thermochromism of a 2D organic–inorganic hybrid perovskite structure based on iodoplumbate and 2-aminomethyl-pyridine
Decarboxylative Halogenation and Cyanation of Electron-Deficient Aryl Carboxylic Acids via Cu Mediator as Well as Electron-Rich Ones through Pd Catalyst under Aerobic Conditions
A simple protocol for Cu-catalyzed protodecarboxylation of (hetero)aromatic carboxylic acids
Facile synthesis of 2,2′-dinitrosubstituted biaryls through Cu-catalyzed ligand-free decarboxylative homocoupling of ortho-nitrobenzoic acids
Recent Progress in Pd-Catalyzed Decarboxylative Coupling Reactions of (Hetero)aromatic Carboxylic Acids
Palladium‐Catalyzed Decarboxylative Methylthiolation of Aromatic Carboxylic Acids by Using DMSO as the Sulfurizing Reagent