Pyrrolo-, pyrazolo- and triazolo-phenanthridines were synthetized by u
sing a Pschorr-type cyclization reaction or an intramolecular cyclizat
ion of arylnitrenium ions. By using these synthetic methods several az
olo-phenanthridines, variously functionalized either in the azolo ring
and in the phenanthridine moiety, were prepared. The title compounds,
tested against murine leukemia eel lines, sensible and multidrug resi
stant, showed moderate activity with IC50 in the range 5-50 mu M.