70400-97-4Relevant 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 13 . Pyrroloindole by Intramolecular Nucleophilic Substitution Reaction in the Pyrrole Series
Aiello, E.,Dattolo, G.,Cirrincione, G.,Almerico, A. M.
, p. 721 - 724 (2007/10/02)
An intramolecular nucleophilic substitution in the pyrrole series has been generalized.The behaviour of nitro, chlorine, bromine and iodine as leaving groups towards the nucleophilic amino group was observed.An acid catalyzed mechanism has been proposed.
POLYCONDENSED NITROGEN HETEROCYCLES. PART XI. 1,3-DISUBSTITUTED 2-METHYLPYRROLOCINNOLINE AND 2-ACETYL-3-METHYLPYRROLOBENZOTRIAZINE
Dattolo, Gaetano,Cirrincione, Girolamo,Almerico, Anna Maria,D'Asdia, Isabella,Aiello, Enrico
, p. 681 - 686 (2007/10/02)
The diazotization of 1,3-disubstituted 2-methyl-5-(2-aminophenyl)pyrroles (2) and the intramolecular coupling reaction of the resulting diazonium salts lead to pyrrolobenzotriazine 4 when R = H.Compound 3d inhibited the germination of seeds
