Title of article :
A New Preparative Route to Substituted Carbazoles by Benzannulation
Author/Authors :
Serra، Stefano نويسنده , , Fuganti، Claudio نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2005
Pages :
-808
From page :
809
To page :
0
Abstract :
A new regioselective pathway to substituted carbazole derivatives is described here. According to this procedure substituted 2-alkoxycarbonyl4-acetoxy-9-(p-toluenesulfonyl) carbazoles are obtained by treatment of substituted 6-[2-(p-toluenesulfonylamino)-aryl]-3-alkoxycarbonylhex-3-en5-ynoic acids with acetic anhydride in the presence of sodium acetate. The latter acids are prepared from the easily available substituted o-iodo-anilines by Sonogashira coupling with propargylic alcohol and Wittig reaction as the key steps. The described benzannulation reaction proceeds in regiospecific fashion and a range of substituents are tolerated.
Keywords :
phenols , carbazoles , Heterocycles , enynes , annulations
Journal title :
Synlett
Serial Year :
2005
Journal title :
Synlett
Record number :
110264
Link To Document :
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