We are engaged in the development of new synthetic strategies for the construction of small organic molecules with broad significance in pharmaceutical and biologically active compound design. Our research aims to address key challenges in modern organic synthesis, with an emphasis on enabling efficient, selective, and modular access to structurally complex and medicinally relevant molecules. Currently, our efforts are focused on three major areas of interest:
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Asymmetric Catalysis
Asymmetric Catalysis
We are developing new asymmetric synthetic methodologies leveraging 3d-transition metal catalysis, with a particular emphasis on copper- and nickel-catalyzed transformations for the efficient construction of enantioenriched organic molecules.
Aminyl Radical Chemistry
Aminyl Radical Chemistry
Our group is focused on developing catalytic methods for the selective generation and utilization of aminyl radicals in organic synthesis, with the goal of enabling new C–N and C–C bond-forming reactions.
Molecular Editing
Molecular Editing
We are also exploring molecular editing strategies for both cyclic and acyclic frameworks, with a particular focus on site-selective bond functionalization and skeletal remodeling relevant to medicinal chemistry.
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