The Journal of organic chemistry

Convergency and Divergency as Strategic Elements in Total Synthesis: The Total Synthesis of (-)-Drupacine and the Formal Total Synthesis of (±)-Cephalotaxine,(-)- …

Q Liu, EM Ferreira, BM Stoltz

Index: Liu, Qi; Ferreira, Eric M.; Stoltz, Brian M. Journal of Organic Chemistry, 2007 , vol. 72, # 19 p. 7352 - 7358

Full Text: HTML

Citation Number: 44

Abstract

A concise route toward the syntheses of (-)-drupacine and (+)-and (-)-cephalotaxine has been developed. The syntheses rely on Pd (II)-catalyzed aerobic oxidative heterocyclization chemistry, which was employed to rapidly construct an important spirocyclic amine intermediate. A dynamic β-elimination/conjugate addition process was strategically applied to complete the first asymmetric total synthesis of (-)-drupacine.

Related Articles:

Solvolytic rearrangement of the 2-(Δ1-cyclopentenyl) ethyl system

[Closson,W.D.; Kwiatkowski,G.T. Tetrahedron, 1965 , vol. 21, p. 2779 - 2789]

Solvolytic rearrangement of the 2-(Δ1-cyclopentenyl) ethyl system

[Closson,W.D.; Kwiatkowski,G.T. Tetrahedron, 1965 , vol. 21, p. 2779 - 2789]

Solvolytic rearrangement of the 2-(Δ1-cyclopentenyl) ethyl system

[Closson,W.D.; Kwiatkowski,G.T. Tetrahedron, 1965 , vol. 21, p. 2779 - 2789]

More Articles...