Over the past few years, isodiazenes have reemerged as a powerful class of intermediates, with a vast synthetic potential. The most direct route to these reactive species is via reactions of N-nucleophiles with nitrenium ion precursors (i.e. anomeric amides). While emerging methodologies are almost exclusively based on amine-derived isodiazenes, analogous transformations based on other nitrogen functionalities (i.e. oximes, heterocycles) are vastly overlooked. Herein, we present a proof-of-principle that the reactivity of nitrenium ion precursors can be expanded beyond its current scope, supported by the development of an unprecedented reaction between anomeric amides and cyclic oximes – isoxazol-5-ones. This unorthodox transformation provides an operationally simple, scalable, and highly chemoselective route to challenging sterically hindered alkynes. Moreover, we demonstrate that anomeric amides can behave as surrogates of nitrous cation.
Ociepa et al. (Fri,) studied this question.