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