A visible light-mediated azidation of α-diazoesters
with
TMSN3 to synthesize valuable α-azidoesters has been
developed. Without using any catalysts and additives, the reaction
proceeded smoothly under visible light irradiation at room temperature.
A variety of α-diazoesters were successfully converted to the
desired α-azidoesters, showing good functional group tolerance.
The products could be readily transformed into triazole, α-azidoacid,
and α-azidoamide. Mechanistic studies suggested that the reaction
is mainly carrying out via direct photoexcitation and SH2 mechanism. This work provides a novel, mild, and practical protocol
for synthesizing α-azidoesters.