The structure of eunicillin (89), a carbobicyclic diterpenoid isolated
from the Mediterranean gorgonian Eunicella stricta, was reported in 1968
(1). At that time chlorine-containing diterpenoids had been dis- covered
in the gorgonian Briareum asbestinum (2, 3), but it was not until 1977
that the structure of the first briaran, briarein A (211), was resolved
by X-ray analysis (4). The first trinervitane diterpenoid (26), which
was isolated from Trinervitermes termites, was reported in 1976 (5). OAc
OAc ACO'---- OH 0 89 211 26 The discovery of these compounds marked the
appearance of a large and growing group of diterpenoids which are
commonly viewed as being formed from cembrane precursors by secondary
carbon-carbon bond closures. It should be emphasized, however, that in
the absence of biosynthetic evidence the question of which groups of
diterpenoids that should be classified as cyclized cembranoids remains
ambiguous. In the present article we have included five tobacco
diterpenoids (1-5) which. possess prerequisite structural features and
co occur with appropriate cembrane precursors in tobacco. Although
structurally reminiscent of cyclized cembranoids, verticillanes, taxanes
and cleomeolide are not dealt with, since these diterpenoids of plant
origin are not believed to arise via preformed cembranoids (6-11).