In 21st century, the development of sustainable and efficient chemical protocols has received considerable attention in the evolution of strategies for organic synthesis. In this context, our group are engaged in discovering the sustainable, effective and highly stereoselective catalytic methodology to construct intricate molecular architectures. Our current research interests include the late-transition-metal catalyzed innate sp3 C-H bond functionalization, other inert chemical bonds activation as well as the organocatalytic tandem reactions for enantiopure biologically important compounds. The research paradigm of our group can be described as the carton.


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