Hippuristanol is a marine derived steroidal natural product
with
promising anticancer activity. However, instability at low pH has
precluded its development as an efficient therapy. We addressed this
limitation by replacing one of the oxygen atoms of the spiroketal
moiety with a carbon atom. Key steps in the synthesis include a Meyer–Schuster/Nazarov
cascade, a hypoiodite mediated oxyfunctionalization, and the late-stage
installation of a hydroxyl group on the C-ring of the steroid.