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          https://www.thieme-connect.de/rss/thieme/de/10.1055-s-00000083.xml
        Synlett  2004(1): 128-130  
DOI: 10.1055/s-2003-44995
   DOI: 10.1055/s-2003-44995
LETTER
© Georg Thieme Verlag Stuttgart · New Yorkl-Proline Promoted Ullmann-Type Coupling Reactions of Aryl Iodides with Indoles, Pyrroles, Imidazoles or Pyrazoles
Weitere Informationen
            
               
                  
                        
                              Received
                              16 October 2003 
                      
Publikationsdatum:
17. Dezember 2003 (online)
            
         
      
   Publikationsverlauf
Publikationsdatum:
17. Dezember 2003 (online)
Abstract
The Ullmann-type coupling reactions of aryl iodides and several nitrogen heterocycles occur at 80-90 °C with l-proline as additive, giving N-arylpyrroles, N-arylindoles, N-arylimidazoles, and N-pyrazoles in good to excellent yields.
Key words
cross coupling - nitrogen heterocycles - catalysis - aryl iodide - additive
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References
For CuI catalyzed coupling reaction of amides with aryl halides under mild conditions, see ref. [5b] . We are investigating this coupling reaction using our conditions and the results will be reported in due course.