The operationally simple method achieves trifluromethylation in imidazopyridines, indicating good functional group compatibility.
A highly efficient, transition‐metal–free trifluoromethylation of imidazopyridines has been achieved using Togni reagent I under simple reaction conditions. This operationally simple method, which employs commercially available reagents, displays good functional group compatibility and a broad substrate scope.
No takes yet. Share an insight, caveat, or question.
Xia et al. (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: