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Reactivity of 4‐chlorobenzo[c][2,7]naphthyridines towards Pd(0) catalyzed coupling reactions and nucleophilic substitutions. aroylation by nucleophilic substitution with analogues of acyl anions
Authors:G Duvey  F Nivoliers  P Rocca  A Godard  F Marsais  G Quguiner
Institution:G. Duvey,F. Nivoliers,P. Rocca,A. Godard,F. Marsais,G. Quéguiner
Abstract:Various 4‐substituted benzoc]2,7]naphthyridines were prepared from the corresponding 4‐chloro derivative by Pd(0) coupling reaction or nucleophilic substitution. More particularly, 4‐aroyl‐benzoe]2,7]naph‐thyridines were synthesized by aroylation with arenecarbaldehydes in the presence of 1,3‐dimethylimida‐zolium iodide.
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