Synfacts 2006(8): 0758-0758  
DOI: 10.1055/s-2006-941938
Synthesis of Natural Products and Potential Drugs
© Georg Thieme Verlag Stuttgart · New York

Synthesis of (±)-Aspidospermidine

Contributor(s): Philip Kocienski, Thomas Snaddon
L. A. Sharp, S. Z. Zard*
École Polytechnique, Palaiseau, France
Further Information

Publication History

Publication Date:
21 July 2006 (online)

Significance

Interest in the synthesis of aspido­spermidine stems from its structural relationship to other important biologically active alkaloids such as vindoline, the lower half of the antitumoral bis-indole alkaloid vinblastine. Sharp and Zard exploited a radical cyclization cascade to efficiently access the core of aspidospermidine in diastereoselective fashion (FI).