Abstract

AbstractA general strategy for synthesis of heterocyclic hemiketal‐containing α,β‐unsaturated ketones has been established. Using the environmentally sound and readily available reagents water and thiourea applied to ynediones, a series of sensitive hemiketals of 3(2 H)‐furanones and 3(2 H)‐thienones were constructed under mild conditions. Both of the reaction conditions are compatible with a diverse range of functional groups. Isotopic labeling, tautomerism, and GC‐MS tracking methods were used to reveal the mechanisms.

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