Formal
total syntheses of stemonamine and cephalotaxine bearing
the core cyclopenta[1,2-b]pyrrolo[1,2-a]azepine ring skeleton were achieved. The general synthetic strategy
in the synthesis features the reductive oxy-Nazarov cyclization as
key step, leading to the versatile construction of N-substituted spiro
quaternary stereogenic centers from readily available starting materials.