Dioxygenation of unprotected mesoionic N-heterocyclic olefins

We report the dioxygenation of mesoionic N-heterocyclic olefins (mNHOs) using molecular dioxygen. For 1,2,3-triazole-derived mNHOs possessing a vinyl proton and at least one acidic C-H group, they are oxidized into the corresponding triazolium benzoate salts, whereas those without vinyl proton or an acidic C-H group are oxidized into triazolium oxide and ketones/aldehydes.

Automated summary

The dioxygenation of mesoionic N-heterocyclic olefins (mNHOs) using molecular dioxygen has been reported. Depending on the presence of a vinyl proton and acidic C-H group, the mNHOs are oxidized into different products.