“…Thus, the condensation of . A. Ogliaruso, M. G. Romanelli, and E. I. Becker benzyl ketone and ethyl phenylglyoxylate with sodium methoxide or the rearrangement and dehydration of 2-oxo-3,4-diphenyl-5-benzoyltetrahydrofuran yields 2,3,5-triphenyl-2-cyclopentene-l,4-dione (CXXXI), the ketonic and stable form of the cyclopentadienone, 2,3,5triphenyl-4-hydroxycyclopentadienone (CXXXII) (28).…”