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Valuable, biologically active chromenones such as those depicted were synthesized based on a diaryl prolinol ether catalyzed, enantioselective reaction of diketones with α,β-unsaturated aldehydes. In these efficient addition–acetalization cascade reactions, diverse aliphatic and aromatic α,β-unsaturated aldehydes, as well as various diketones, can be successfully applied and the 2-hydroxychromenones can be isolated in good yields and with excellent enantioselectivities.
Rueping et al. (Tue,) studied this question.