A visible-light-induced radical gem-iodoallylation
of CF3CHN2 was developed under mild conditions,
delivering a variety of α-CF3-substituted homoallylic
iodide compounds in moderate to excellent yields. The transformation
features broad substrate scope, good functional group compatibility,
and operational simplicity. The described protocol provides a convenient
and attractive tool to apply CF3CHN2 as CF3-introduction reagent in radical synthetic chemistry.