Preparative synthesis of a new, soluble, and functionalized buckybowl is described. The precursor of dibenzo[g,p]chrysene having four bromine atoms at two fjord regions undertook palladium-catalyzed intramolecular cyclization to afford a skeletal buckybowl, namely, diindeno(1,2,3,4-defg:1',2',3',4'mnop)chrysene. The resulting curved scaffold possesses two important substituents: four-fold alkyls increasing solubility and four-fold methoxy groups that could be further functionalized. These two features, coupled with the gently curved π-system, enable general access to solution-compatible and multi-functional buckybowl molecules.