Area of research
Materials Chemistry · Molecular Biology
Research interest
Research focused on Intramolecular force and Regioselectivity, with related work in Combinatorial chemistry, Domino, Ugi reaction. Notable publications include 'A Diversity‐Oriented Approach to Spiroindolines: Post‐Ugi Gold‐Catalyzed Diastereoselective Domino Cyclization', 'Design of a Bioactive Small Molecule That Targets the Myotonic Dystrophy Type 1 RNA via an RNA Motif–Ligand Database and Chemical Similarity Searching', and 'Switching the regioselectivity via indium(iii) and gold(i) catalysis: a post-Ugi intramolecular hydroarylation to azepino- and azocino-[c,d]indolones'.
Long‐term exposure to indoor air pollution and risk of tuberculosis
Regioselective Synthesis of Diversely Substituted Diazoninones Through a Post‐Ugi Gold‐Catalyzed Intramolecular Hydroarylation Process
Switching the regioselectivity via indium(iii) and gold(i) catalysis: a post-Ugi intramolecular hydroarylation to azepino- and azocino-[c,d]indolones
An Expedient Route to Imidazo[1,4]diazepin-7-ones via A Post-Ugi Gold-Catalyzed Heteroannulation
Post-Ugi gold-catalyzed diastereoselective domino cyclization for the synthesis of diversely substituted spiroindolines
Diversely Substituted Triazolo[1,5‐<i>a</i>][1,4]benzodiazepinones: A Post‐Ugi Copper‐Catalyzed Tandem Azide–Alkyne Cycloaddition/Ullmann C–N Coupling Approach
Post Ugi Gold(I)- and Platinum(II)-Catalyzed Alkyne Activation: Synthesis of Diversely Substituted Fused Azepinones and Pyridinones
Gold(I)‐Catalyzed Post‐Ugi Hydroarylation: An Approach to Pyrrolopyridines and Azepinoindoles
A Diversity‐Oriented Approach to Spiroindolines: Post‐Ugi Gold‐Catalyzed Diastereoselective Domino Cyclization
Design of a Bioactive Small Molecule That Targets the Myotonic Dystrophy Type 1 RNA via an RNA Motif–Ligand Database and Chemical Similarity Searching
Gold(i) and platinum(ii) switch: a post-Ugi intramolecular hydroarylation to pyrrolopyridinones and pyrroloazepinones