Homoallylic o-halobenzylamines: asymmetric diversity-oriented synthesis of benzo-fused cyclic amines

Abstract

The presence of a halogen atom in the proximity of a homoallylic amine, obtained by asymmetric addition of allylzinc bromide to the corresponding tert-butyl sulfinimine, makes them versatile building blocks suitable to participate in several palladium-catalyzed processes, such as the intramolecular Heck reaction or the Sonogashira cross-coupling. The thus obtained ortho-alkynyl derivatives display two unsaturated functional groups which may be further modified by means of the intramolecular Pauson–Khand reaction or the ring-closing enyne metathesis. In this way, a variety of benzo-fused amines can be obtained in 2–3 steps from readily available starting materials.