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Access to unsaturated bicyclic lactones by overriding conventional C(sp3)–H site selectivity - Nature Chemistry

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Access to unsaturated bicyclic lactones by overriding conventional C(sp3)–H site selectivity - Nature Chemistry

Transition metal catalysis plays a pivotal role in transforming unreactive C–H bonds. However, regioselective activation of distal aliphatic C–H bonds poses a tremendous challenge, particularly in the absence of directing templates. Activation of a methylene C–H bond in the presence of methyl C–H is underexplored. Here we show activation of a methylene C–H bond in the presence of methyl C–H bonds to form unsaturated bicyclic lactones.

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Access to unsaturated bicyclic lactones by overriding conventional C(sp3)–H site selectivity - Nature Chemistry

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Access to unsaturated bicyclic lactones by overriding conventional C(sp3)–H site selectivity - Nature Chemistry

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