A rapid synthetic entry towards the pseudopterosins, a class of diterp
enes which display potent anti-inflammatory and analgesic properties,
is described. The key feature of this approach is the use of a sequent
ial intramolecular, Lewis acid mediated Friedel-Crafts alkylation - Fr
iedel-Crafts acylation sequence, viz 14 to 15, to establish the tricyc
lic carbon framework.