Our group is focused on the development of innovative asymmetric synthetic methodologies, grounded in the reactivity of radical intermediates. Our research harnesses electrochemical activation as a central tool to generate and control open-shell species in a selective and sustainable manner. By combining radical chemistry with modern organocatalysis, we design strategies that enable the efficient and stereoselective construction of complex molecular architectures.
Our approach spans both catalytic and non-catalytic systems, with a particular emphasis on enantioselective transformations. Most of our catalytic work relies on small organic molecules as chiral catalysts, offering operational simplicity, broad functional group tolerance, and precise stereochemical control. Through this lens, we seek to tackle key challenges in modern synthesis — such as reactivity under mild conditions, selectivity, and sustainability.
While electrochemistry is our primary activation mode, we also investigate photochemical methods when synergistic or complementary to our electrochemical platforms. These dual approaches allow us to expand the reactivity landscape of radicals and explore novel mechanisms.
Our broader goal is to establish a versatile, scalable, and environmentally conscious radical-based platform for asymmetric synthesis, with applications ranging from drug development to materials science. We adopt a multidisciplinary mindset, integrating insights from physical organic chemistry, reaction design, and green chemistry principles.