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(10): 1048-1048  
DOI: 10.1055/s-2006-949311
   DOI: 10.1055/s-2006-949311
Metal-Mediated Synthesis
© Georg Thieme Verlag Stuttgart · New YorkCo-Catalyzed Conjugate Addition of Aryl Halides to Activated Olefins
M. Amatore, C. Gosmini*, J. Périchon
Université Paris 12, Thiais, France
Further Information
            
               
                  
            
         
      
   Publication History
Publication Date:
21 September 2006 (online)
Significance
The conjugate addition of organometallic reagents to the double bond of electron-deficient olefins is a very powerful method of the formation of new C-C bonds. The authors developed a novel, very simple and convenient method of direct addition of aryl halides, including chlorides, and triflates to Michael acceptors like acrylonitrile and acrylate esters. Inexpensive cobalt bromide and 2,2′-bipyridine are used as catalysts. The reaction gives good yields both for electron-rich and electron-poor arenes and tolerates a number of functional groups.