Transition-Metal-Catalyzed Asymmetric Synthesis of Bicyclo[3.3.1]nonane Frameworks

Bing Liu1, Tingyuan Zheng1, Jiahui Cheng1

  • 1Research Institute for Doping Control, Shanghai University of Sport, Shanghai, China.

Summary

Transition-metal catalysis offers efficient and selective routes to bicyclo[3.3.1]nonanes, crucial scaffolds in drug discovery. This review highlights advances in palladium, rhodium, and copper-catalyzed asymmetric synthesis for these complex structures.

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