Highly Stereoselective and Scalable Synthesis of <i>trans</i>-Fused Octahydrocyclohepta[<i>b</i>]pyrrol-4(1<i>H</i>)‑ones via the Aza-Cope–Mannich Rearrangement in Racemic and Enantiopure Forms

We have developed an efficient and stereoselective route to trans-fused octahydrocyclohepta­[b]­pyrrol-4­(1H)-ones. The key features of our synthesis include the regioselective epoxide ring-opening of alkynyl oxiranes and a stereoselective aza-Cope–Mannich reaction. The target compounds were prepared in 3–6 steps from commercially available starting materials (61–75% overall yield) with minimal chromatographic purification. We have devised an stereoselective route to target compounds using Shi epoxidation or (R)-1-phenylethylamine as a source of chirality.