Anion assisted [4 + 2] cycloaddition reaction via indolo[2,3]-dienolate by reacting 1,2-dimethylindole-3-carboxaldehyde with aromatic nitriles using lithium diisopropylamide in terahydrofuran, a facile and convenient regiospecific route designed and developed for the synthesis of γ-carbolines.

Molecules possessing harmine moiety are reported to exhibit marked fungicidal and bactericidal activities. In this study, various quinozilinium tetrafluoroborate salts were synthesized using acylic and cyclic oxoketene dithioacetals followed by cycloaromatization from Harmine. All of these synthesized compounds were characterized by 1H NMR, 13C NMR, Mass and CHN analysis. This methodology would find wide usage in the preparation of indolo quinozilinium -based library of small molecules useful for medicinal chemistry and in drug discovery.