Catalytic electron donor–acceptor complex triggered cascade radical trifluoromethylation/cyclization of N-isopentenyl aldehyde hydrazones
Abstract
Photocatalytic trifluoromethylation/cyclization of N-isopentenyl aldehyde hydrazones triggered by a catalytic electron donor–acceptor (EDA) complex was developed for the construction of C5-trifluoromethylated tetrahydropyridazines. A catalytic amount of tris(4-bromophenyl)amine was used as the electron donor with trifluoromethyl thianthrenium triflate as the acceptor to generate a trifluoromethyl radical after irradiation. This environmentally benign methodology eliminates the need for a photocatalyst, offering a straightforward and efficient approach to accessing C5-trifluoromethylated tetrahydropyridazines.

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