Front Cover: Development of Organoautocatalyzed Double s-Bond C(sp2)-N Transamination Metathesis Reaction (Angew. Chem. Int. Ed. 28/2025)
Graphical Abstract
Organoautocatalyzed transamination metathesis of challenging cyclic tertiary amines is reported. In their Research Article (e202505275), Svetlana B. Tsogoeva and co-workers demonstrate the use of an in situ-formed pyrrolidinium salt as an efficient organoautocatalyst, enabling double C(sp2)-N bond metathesis at room temperature via a domino reaction mechanism. This metal- and additive-free transformation advances green, waste-reducing, and sustainable approaches in organic synthesis.