Chemical communications | 2021

Dioxygenation of unprotected mesoionic N-heterocyclic olefins.

 
 
 
 

Abstract


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.

Volume None
Pages None
DOI 10.1039/d1cc04695k
Language English
Journal Chemical communications

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