Shows effective lactone synthesis using an intramolecular approach, indicating robust diastereoselectivity.
), a sterically bulky achiral catalyst, was found to enable the formation of lactones. Alkyl γ-lactones were synthesized in excellent yields and diastereoselectivity, and a diverse array of disubstituted lactones (γ, δ, and ε) were synthesized with good yields and diastereoselectivity. This chemistry was extended to intramolecular C-H insertion in late-stage functionalization with excellent regio- and diastereoselectivity.
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Bagale et al. (2026) studied this question.
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