Convenient access to 1, 3, 5-triaroylbenzenes
…, R Jankowski, D Prim, J Mahuteau, A Chiaroni
Index: Joseph, Delphine; Jankowski, Raphael; Prim, Damien; Mahuteau, Jacqueline; Chiaroni, Angele Tetrahedron Letters, 2002 , vol. 43, # 45 p. 8051 - 8054
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Citation Number: 9
Abstract
The unusual transformation of β-aryl-β-haloacroleins into valuable triaroylbenzenes is reported by the first time. The convenient sequence takes advantage on the one step access to triaroylbenzenes. This work establishes that the presence of amine is required for the trimerization procedure since it is involved in the formation of iminium–enamine intermediate A.
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