Photocatalytic Strategies for the Functionalization of Pyridines

Identificador:  TDX:4150

Handle: https://hdl.handle.net/20.500.11797/TDX4150

Autores:  Georgiou, Eleni

Resumen:
The aim of this research was to develop new photocatalytic strategies for the functionalization of pyridines. Given the importance of these structural motifs in pharmaceuticals and other sectors of the chemical industry, developing new catalytic pyridine functionalization processes which expand upon known methodologies and overcome current limitations is of extreme value. Towards this end, we initially developed a switchable photocatalytic system that granted access to C4 and C2 benzylated cyanopyridines. The two processes used the same reaction conditions and photoredox catalysts, and differed only in the nature of the photochemical quencher, which allowed us to select at will between mechanistically divergent processes. The two reaction manifolds, an ipso-substitution path proceeding via radical coupling and a Minisci-type addition, enabled selective access to regioisomeric C4 or C2 benzylated pyridines, respectively. In a second project, we devised a new photocatalytic procedure for the C-H allylation of pyridines. This method overcame several of the current methodologies’ limitations, including the need for the prefunctionalization of the pyridine substrates. The method allows the functionalization of pyridines with radicals derived from allylic C-H bonds. Overall, two substrates undergo C-H functionalization to form a new C(sp2)-C(sp3) bond. A dithiophosphoric acid organocatalyst was crucial to master three catalytic functions, sequentially acting as: i) a Brønsted acid, ii) a single electron reductant, and iii) a hydrogen atom abstractor for the activation of allylic C-H bonds. The resulting pyridinyl and allylic radicals then couple with high regioselectivity. Taken together, these methodologies offer new strategies for the selective functionalization of pyridines and have been successfully applied for the late-stage diversification of valuable molecules, including marketed drugs. These strategies require mild operational conditions and simple visible light illumination, and, because of their utility for the rapid and selective functionalization of valuable pyridine scaffolds, they have the potential to be quickly adopted by chemists.