Second-Generation Enantioselective Synthesis of the Tricyclic ABC Core of Daphnicyclidin A.

Key Points

• The aim is to develop a robust method for the enantioselective synthesis of the tricyclic ABC core of daphnicyclidin A.
• Utilized second-generation techniques for synthesis
• Focused on enantioselective processes for alkaloids
• Explored the robustness and utility of the methods in synthesis
• Achieved efficient enantioselective synthesis of the tricyclic core
• Demonstrated significant utility for novel alkaloid synthesis