Total synthesis of gracilamine

The total synthesis of gracilamine, a pentacyclic Amaryllidaceae alkaloid, was achieved from simple building blocks. The synthesis features a mild photo-Nazarov reaction, intramolecular 1,4-addition, and an intramolecular Mannich reaction. This approach not only confirms the C6 stereochemistry of natural gracilamine, and also provides a novel solution to prepare its derivatives and structurally related natural products. Simple building blocks were employed in the total synthesis of gracilamine, a pentacyclic Amaryllidaceae alkaloid. The synthesis features a mild photo-Nazarov reaction, intramolecular 1,4-addition, and an intramolecular Mannich reaction. This strategy provides a novel approach to prepare gracilamine derivatives and structurally related natural products.