1407547-40-3Relevant academic research and scientific papers
Highly stereoselective and scalable synthesis of trans -fused octahydrocyclohepta[ b ]pyrrol-4(1 H)-ones via the aza-Cope-Mannich rearrangement in racemic and enantiopure forms
Belov, Dmitry S.,Lukyanenko, Evgeny R.,Kurkin, Alexander V.,Yurovskaya, Marina A.
, p. 10125 - 10134 (2013/01/15)
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 r
