Formal cycloaddition synthesizes all-carbon bridged bicyclo[5.1.1]nonanones, suggesting a versatile method in organic synthesis.
A formal (5+3) cycloaddition of bicyclo[1.1.0]butanes (BCBs) with maltol derivatives is achieved by employing oxidopyrylium species as 1,5-dipoles. This transformation provides a new pathway for synthesizing all-carbon bridged bicyclo[5.1.1]nonanones, a structurally constrained medium-ring scaffold. The reaction proceeds under mild conditions and exhibits high functional group tolerance alongside a broad substrate scope.
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Yan et al. (2026) studied this question.
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