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  2010(9): 1042-1042  
DOI: 10.1055/s-0030-1257958
   DOI: 10.1055/s-0030-1257958
Metal-Catalyzed Asymmetric Synthesis and Stereoselective Reactions
© Georg Thieme Verlag
      Stuttgart ˙ New YorkSynthesis of Azetidines through an Oxidative Cyclization
Y. Ye, H. Wang, R. Fan*
Fudan University, Shanghai, P. R. of China
Further Information
            
               
                  
            
         
      
   Publication History
Publication Date:
23 August 2010 (online)

Significance
This work describes the synthesis of azetidines through an oxidative hypervalent iodine mediated cyclization of Michael adducts. Azetidines are an important class of heterocycles commonly found in natural products and drug targets (see Review below). This work follows the group’s earlier reports on similar cyclizations yielding other heterocycles. The scope of aromatic substituents is general and the products are obtained in good overall yield and high diastereoselectivity.
 
    