Synthetic secofriedelane and friedelane derivatives as inhibitors of humanlymphocyte proliferation and growth of human cancer cell lines in vitro

Controlled silylation of friedelin (1) from cork smoker wash solids, a bypr oduct generated during processing of corkboard by steam baking, gave 3-trim ethylsiloxyfriedel-2-ene (3) in high yields. Oxidation of 3 with OsO4/NMMO produced 2 alpha -hydroxyfriedelan-3-one (cerin) (5), from which the new 2, 3-secofriedelan-2-al-3-oic acid (6) was obtained quantitatively by periodic acid oxidation. Oxidation of 3 with DDQ afforded friedel-1-en-3-one (8). R eductive ozonolysis of 3 gave 2 alpha ,3 beta -dihydroxyfriedelane, pachysa ndiol A (7). Compound 6 proved to be a potent inhibitor of human lymphocyte proliferation (IC50 = 10.7 muM) and of the growth of a human cancer cell l ine (GI(50) = 5.4-17.2 muM). C-13 NMR data for compounds (3, 4, 5, 6a, 7, a nd 8) are described for the first time.