A thermal dipolar cycloaddition and rearrangement reaction to form pyrrolines has been redirected towards the synthesis of γ-keto- and γ-aldoamides from nitrones and ynamides with a Cu(II) catalyst. A copper-coordinated iminium intermediate is proposed to initiate a diastereoselective rearrangement for C–C bond formation and a combination of catalyst and nitrone protecting group balance the desired reactivity, diastereoselectivity, and sensitivity to hydrolysis. Reaction optimization is described in addition to scope, mechanistic studies, and conversion of γ-ketoamides to 1,4-diones. This catalytic method showcases distinct copper-catalyzed reactivity of N-alkenylnitrones for the synthesis of 1,4-dicarbonyl compounds.
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Alshreimi et al. (2024) studied this question.
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