We here describe a new Cu-catalyzed annulation cascade of alkyne-tethered α-bromocarbonyls with common alkynes for the synthesis of various heteropolycycle frameworks, including 1 H -benzo[ de ]quinolin-2(3 H )-ones, 4 H -dibenzo[ de,g ]quinolin-5(6 H )-one, and benzo[ de ]chromen-2(3 H )-one, which were constructed with high selectivity. This was achieved by two-component annulation cascades, rather than atom-transfer radical cyclization (ATRC), with alkyne-tethered α-bromocarbonyls for one-step accessing heteropolycycles via C–Br bond split, intramolecular cyclization, intermolecular [4 + 2] annulation, and aryl C(sp 2 )–H functionalization cascades.