77411-80-4Relevant academic research and scientific papers
A new entry to the substituted pyrrolo[3,2-c]quinoline derivatives of biological interest by intramolecular heteroannulation of internal imines
Testa, Maria Luisa,Lamartina, Liliana,Mingoia, Francesco
, p. 5873 - 5880 (2007/10/03)
New 1,3,4-substituted pyrrolo[3,2-c]quinoline derivatives were synthesised in good yields by oxidative heteroannulation of internal imines starting from easily prepared substituted 5-(2-aminophenyl)pyrroles and commercially available aryl and heteroaryl a
Polycondensed Nitrogen Heterocycles. Part 8. Pyrroloindole
Aiello, Enrico,Dattolo, Gaetano,Cirrincione, Girolamo
, p. 1 - 3 (2007/10/02)
The reduction of the nitro-derivatives (4a-c) with iron-acetic acid leads to the pyrroloindoles (7a-c).This unusual indolization, in which displacement of the heterocycle amino-group occurs, is regarded as a nucleophilic attack by the 2-aminophenyl
