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The title compounds were reacted with a few conjugated dienes at room temperature and above. The alcohols were unreactive, but the other ynones reacted at a reasonable rate. Conceivably, the expected cyclohexa-1,4-diene adducts were formed, but they were unstable and aromatized to the corresponding benzene derivatives, which were isolated in low to excellent yield.

Diels-Alder reactions with 1,1-diethoxybut-3-yn-2-one and some 1,1-diethoxy-5-hydroxyalk-3-yn-2-ones and their acetates