Area of research
Organic Chemistry · Spectroscopy
Research interest
Research interests include Chemistry, Alkyl, Regioselectivity, Catalysis, Flavones, and Surface modification.
Myricetin Suppresses Inflammatory Th17 Polarization to Mitigate Alzheimer's Disease Pathogenesis
Electrochemical phosphorylation of arenols and anilines leading to organophosphates and phosphoramidates
Using SeO<sub>2</sub>as a selenium source to make RSe-substituted aniline and imidazo[1,2-<i>a</i>]pyridine derivatives
<scp>d</scp> -Sedoheptulose-7-phosphate is a common precursor for the heptoses of septacidin and hygromycin B
Copper-catalyzed generation of flavone selenide and thioether derivatives using KSeCN and KSCN <i>via</i> C–H functionalization
Nickel-catalyzed C(sp2)-H selenation of imidazo[1,2-α]pyridines with arylboronic acids or alkyl reagents using selenium powder
New polycyclic tetramate macrolactams from marine-derived Streptomyces sp. SCSIO 40060
One-pot synthesis of glycosyl phenylthiosulfonates from sulfinate, S and glycosyl bromides
One‐Pot Three‐Component Synthesis of Alkylthio‐/Arylthio‐ Substituted Imidazo[1,2‐<i>a</i>]pyridine Derivatives <i>via</i> C(<i>sp</i><sup>2</sup>)–H Functionalization
Making Flavone Thioethers Using Halides and Powdered Sulfur or Na<sub>2</sub>S<sub>2</sub>O<sub>3</sub>
Synthesis of imidazol[1,2-α]pyridine thioethers via using sulfur powder and halides as reactants
“One-pot” sequential preparation of isoquinoline-1,3(2H,4H)-dione derivatives by reacting N-alkyl(aryl)-N-methacryloyl benzamides with benzyl alcohols and sodium benzenesulfinates
Cu-catalyzed sulfenylation of imidazol[1,2-a]pyridine via C–H functionalization using a combination of Na<sub>2</sub>S<sub>2</sub>O<sub>3</sub> and halides
Ammonium Iodide Induced Nonradical Regioselective Sulfenylation of Flavones via a C–H Functionalization Process
Regioselective Cross-Couplings of Coumarins and Flavones with Ethers via C(sp<sup>3</sup>)–H Functionalization
Cascade Couplings of <i>N</i>-Alkyl-<i>N</i>-methacryloyl Benzamides with Ethers and Benzenesulfonohydrazides To Generate Isoquinoline-1,3(2<i>H</i>,4<i>H</i>)-dione Derivatives
Generation of thioethers via direct C–H functionalization with sodium benzenesulfinate as a sulfur source
Recent Progress towards Transition‐Metal‐Catalyzed Synthesis of Fluorenes
Regioselective C−S Bond Formation between Flavones and Arylsulfonyl Chlorides through the Use of Ammonium Iodide
Generation of ArS-substituted flavone derivatives using aryl thiols as sulfenylating agents
Copper-catalyzed oxidative cascade coupling of N-alkyl-N-phenylacrylamides with aryl aldehydes
Synthesis of isoquinoline-1,3(2H,4H)-dione derivatives via cascade reactions of N-alkyl-N-methacryloyl benzamide with aryl aldehydes
Metal-free syntheses of oxindole derivatives via a benzoylation/substitution/desulfonylation/cyclization cascade
Syntheses of five- and seven-membered ring sultam derivatives by Michael addition and Baylis–Hillman reactions
Selective Synthesis of Seven- and Eight-Membered Ring Sultams via Two Tandem Reaction Protocols from One Starting Material
Multicapillary Flow Reactor: Synthesis of 1,2,5-Thiadiazepane 1,1-Dioxide Library Utilizing One-Pot Elimination and Inter-/Intramolecular Double aza-Michael Addition Via Microwave-Assisted, Continuous-Flow Organic Synthesis (MACOS)