A convenient synthesis of cytotoxic pyrroloquinazolinoquinoline alkaloid, l
uotonin A (1), was achieved in 3 steps; (i) reaction of anthranilic acid wi
th O-methylbutyrolactim to deoxyvasicinone, (ii) oxidation of deoxyvasicino
ne, and (iii) formation of luotonin A by the reaction of vasicinone with an
thranyl aldehyde.