Copper-mediated trifluoromethylation expands access to sp2-trifluoromethylated cyclopropenes, suggesting new synthetic avenues.
Cyclopropenes are the smallest unsaturated carbocycles. They possess exceptionally high ring strain, resulting in unique reactivity, enabling C=C bond functionalization and ring-opening transformations. Herein, we report a copper-mediated trifluoromethylation of cyclopropenyl benziodoxole (CpBX) reagents, providing access to previously inaccessible, yet highly useful, sp2-trifluoromethylated cyclopropenes. Subsequent functionalizations of these novel strained ring building blocks enabled access to highly-substituted trifluoromethylated cyclopropanes, difluoromethylene cyclopropanes and non-cyclic trifluoromethylated compounds.
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Wu et al. (2025) studied this question.
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