Intramolecular N-acyliminium ion versus Friedel-Crafts cyclization onto 3-indoles: synthesis of the novel rings pyrrolizino[2,1-b]indole and homologues

摘要

Acid treatment of indole-2-carboxylic acid beta- and gamma-oxoamides causes Friedel-Crafts intramolecular cyclization to beta-carbolinones and dihydro-2H-azepino[3,4-b]indol-1-ones, in contrast to secondary delta-, epsilon- and zeta-oxoamides, which cyclize to the novel heterocyclic rings pyrrolizino[2,1-b]indole, indolizino[2,1-b]indole, and 9a,11-diaza-indeno[1,2-a]azulene, via an intermediate N-acyliminium ion. Tertiary amides lead only the Friedel-Crafts ring closure, thus allowing the synthesis of larger fused rings.