“…Evaporation of the solvent yielded a 2:1 mixture of 8 and 11; prolonged reaction did not lead to a change in the ratio OH NMR) (no isomerization was observed in the absence of iodine). Chromatography of the equilibrium mixture on silica gel (45 X 2.5 cm column) with benzene-ethyl acetate (2:1) afforded pure 11 (eluted before 8), recrystallized from ether-petroleum ether: yield 100 mg (27%); mp 106-107 °C (depressed by an admixture of 8); IR (KBr) 1760 (s), 1725 (s), 1655 (s) cm'1; UV (CH3OH) X^3 07 nm (e 14000), XmM 308 nm in dimethyl sulfoxide; 'H NMR (CDC13)…”