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        Synthesis  2010(3): 510-514  
DOI: 10.1055/s-0029-1217114
   DOI: 10.1055/s-0029-1217114
PAPER
© Georg Thieme Verlag
      Stuttgart ˙ New YorkSynthesis of β-Arylporphyrins and Oligophenylenediporphyrins by the Suzuki-Miyaura Reaction
Further Information
            
               
                  
                        
                              Received
                              9 September 2009 
                      
Publication Date:
20 November 2009 (online)
            
         
      
   Publication History
Publication Date:
20 November 2009 (online)

Abstract
Several β-aryl-substituted porphyrins were prepared in good yields by Suzuki-Miyaura cross-coupling of 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5,10,15,20-tetraphenylporphinatozinc(II) with various aryl bromides. Additionally, syntheses of β,β′-diporphyrins linked by biphenylene or quaterphenylene units were examined.
Key words
Suzuki-Miyaura reaction - cross-coupling - oligophenylenes - porphyrins - coupling
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