Area of research
Organic Chemistry · Inorganic Chemistry
Research interest
Research interests include Chemistry, Catalysis, Desymmetrization, Enantioselective synthesis, Stereoselectivity, and Stereochemistry.
Desymmetrizing atroposelective bromination of N-arylcarbazoles enabled by cross-assembled bifunctional catalysts
Organocatalytic diastereo- and atroposelective construction of N–N axially chiral pyrroles and indoles
Enantioselective Access to Triaryl-2-pyrones with Monoaxial or Contiguous C–C Diaxes via Oxidative NHC Catalysis
Targeting Pathogenic Formate-Dependent Bacteria with a Bioinspired Metallo–Nitroreductase Complex
Organocatalytic cycloaddition of alkynylindoles with azonaphthalenes for atroposelective construction of indole-based biaryls
Construction of Axially Chiral Compounds via Central‐to‐Axial Chirality Conversion
Application of Halogen Bonding to Organocatalysis: A Theoretical Perspective
Diastereo- and Atroposelective Synthesis of Bridged Biaryls Bearing an Eight-Membered Lactone through an Organocatalytic Cascade
Conversion of two stereocenters to one or two chiral axes: atroposelective synthesis of 2,3-diarylbenzoindoles
Enantioselective [3 + 2] Formal Cycloaddition of 1-Styrylnaphthols with Quinones Catalyzed by a Chiral Phosphoric Acid
Enantioselective Organocatalytic Sulfenylation of β-Naphthols
Desymmetrizing Enantio- and Diastereoselective Selenoetherification through Supramolecular Catalysis
Asymmetric Arylative Dearomatization of β‐Naphthols Catalyzed by a Chiral Phosphoric Acid
N‐Heterocyclic Carbene‐Catalyzed Intramolecular Nucleophilic Substitution: Enantioselective Construction of All‐Carbon Quaternary Stereocenters
Multiphoton harvesting metal–organic frameworks
Chiral Phosphoric Acid Catalyzed Highly Enantioselective Desymmetrization of 2-Substituted and 2,2-Disubstituted 1,3-Diols via Oxidative Cleavage of Benzylidene Acetals
<i>N</i>-Heterocyclic Carbene Catalyzed Intramolecular Acylation of Allylic Electrophiles
Oxyanion Hole Stabilization by C–H···O Interaction in a Transition State—A Three-Point Interaction Model for<i>Cinchona</i>Alkaloid-Catalyzed Asymmetric Methanolysis of<i>meso</i>-Cyclic Anhydrides