Synthesis of cananodine by intramolecular epoxide opening

Tetrahedron Lett. 2017 Aug;58(35):3478-3481. doi: 10.1016/j.tetlet.2017.07.080. Epub 2017 Jul 25.

Abstract

Cananodine is a guaipyridine alkaloid with activity against liver cancer. Cananodine was synthesized using a remarkable intramolecular opening of a trisubstituted epoxide as the key step in construction of the seven-membered carbocycle of the target. The epoxide opening strategy allows all four stereoisomers of cananodine to be prepared.