of main observation and conclusion A total synthesis of 6,7,9,10,12,12a-hexahydro-2-methyl-(2R,4aS,12aS)-2H,5H-benzo[e]pyrrolo-[3,2,1-ij]quinolone-4,11(1H,3H)-dione (1), a unique pyrroloquinolone-type Lycopodium alkaloid containing a complex 6/6/6/5 tetracyclic core, has been disclosed in eight steps and 38% overall yield. The reported synthesis features a short, efficient synthesis of the crucial multi-substituted cyclohexanone intermediate with three stereogenic centers, and one-pot generation of the complex 6/6/6/5 tetracyclic core in a single tandem step.