Abstract:The synthesis of substituted 1-benzyl-1H-pyrrolo[2,3-b]pyridines and 5-benzyl-5H-pyrrolo-[2,3-b]pyrazines has been performed by cycloisomerization of the corresponding N-benzyl-3-alkynyl-5-arylpyridin(or pyrazin)-2-yl amines with AuCl 3 . Alkynylamines have been obtained starting from 3-bromo-5-substituted N-(pyridin-or pyrazin-2-yl)pyridinium aminides in a regioselective way.
Differently modified 2-aminopyridines and pyrazines bearing an arylazo group at the 3-or 5-position have been generated from pyridinium N-aminides in a regioselective fashion. The detailed chemistry starts with attack of the N-aminide
Differently modified 2-aminopyridines and pyrazines bearing an arylazo group at the 3-or 5-position have been generated from pyridinium N-aminides in a regioselective fashion. The detailed chemistry starts with attack of the N-aminide
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