Intramolecular cascade rearrangements of enynamine derived ketenimines: access to acyclic and cyclic amidines

Abstract

Copper-catalyzed reaction of enynamines with sulfonylazides provides acyclic and cyclic amidines. Nucleophilic addition of the tethered amino group on the in situ generated ketenimine forms a six-membered cyclic zwitterionic intermediate which facilitates migration of the tethered amino group to the C-center giving the acyclic amidine. On the other hand, migration of a substituent on the amino group to C- and C-centers results in the formation of cyclic amidines. Computational studies were carried out to validate the mechanism which indicates that the product distribution of the process depends on the substitutions on the enynamine backbone.

o-Silylaryl Triflates: A Journey of Kobayashi Aryne Precursors

“…Later in 2018, another [4 + 2]/[2 + 2] cycloaddition reaction process was reported by Wang and co-workers, in which the generated [4 + 2] cycloadducts 4-159 from compounds 4-157 could react with arynes to afford 4-158 via the [2 + 2] cycloaddition reaction (Scheme b) . Other [2 + 2] cycloaddition reactions between o -silylaryl triflates and simple olefins were also explored. , …”