A formal synthesis of pseudolaric acid B, a diterpene isolated from the root bark
of Pseudolarix kaempferi Gordon (Pinaceae), to Trost’s synthetic intermediate was achieved in 17 steps from
a known ketone. Key features of this synthesis include a Claisen rearrangement and
iodoetherification to construct quaternary stereocenters and ring-closing metathesis
to form the seven-membered ring.
Key words
pseudolaric acid B - total synthesis - diterpenes - cytotoxins - Claisen rearrangement
- iodoetherification