An　efficient　and　user-friendly　synthesis　of　7H-chromeno[3,2-c]　quinolines　has　been　developed　via　a　one-pot　oxidative　O-arylation,　Pdcatalyzed　C(sp(3))-H　arylation　of　readily　available　arylols　and　trivalent　aryliodine　reagents.　A　variety　of　valuable　and　complex　fused　heterocycles　were　quickly　assembled　in　high　isolated　yields　with　broad　substrate　scopes.