The bulk industrial chemical 2-bromo-3,3,3-trifluoropropene (BTP) was first employed as a coupling partner in photocatalytic defluorinative reactions with N-aryl amino acids. Photoredox activation of the C(sp 2 )−Br bond of the resultant 2bromo-1,1-difluoroalkenes generates gem-difluoro vinyl radicals for further radical cyclization. Various 4-(difluoromethylidene)-tetrahydroquinolines were assembled in good yields by combining two photoredox cycles with a single photocatalyst.2,3-Dihydroquinolones, the aza-analogues of flavanones, are compounds of considerable interest because of their manifold biological properties, such as antiulcer, anti-inflammatory, and antitumor (Figure 1). 1 However, the carbonyl group is