A concise total synthesis of (+)-propindilactone G, a nortriterpenoid isolated from the stems of
Schisandra propinqua var
. propinqua, has been achieved for the first time. The key steps include an asymmetric Diels–Alder reaction, a Pauson–Khand reaction, a Pd-catalyzed reductive hydrogenolysis reaction, and an oxidative heterocoupling reaction. These reactions enabled the synthesis in only 20 steps. As a consequence of our synthetic studies, the structure of propindilactone G has been revised. More information can be found in their Full Papers on pages 1406, 1414, and 1425 by Zhen Yang and Jia-Hua Chen et al.
in Issue 9, 2016 (DOI:
10.1002/asia.201600129,
10.1002/asia.201600130,
10.1002/asia.201600131.).