The first sequential acid-catalyzed propargylation/base-mediated aza-cycloisomerization between indolyl-benzimidazoles and
propargylic alcohols is described. This protocol enables the one-pot
construction of N-fused benzimidazo-β-carbolines
in good yields. The synthetic utility of this approach is demonstrated
by the assembly of an aza-helicene and also by a gram-scale reaction.