Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
          
          https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000131.xml
        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 YorkSynthesis 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).
 
    