Direct alkynylation of C(sp3)–H bonds in cyclobutane carboxamides shows promise for streamlined synthesis, suggesting potential in organic chemistry.
The direct functionalization of C(sp³)-H bonds assisted by native carbonyl functional groups is a promising strategy for the streamlined synthesis of complex molecules. Here, we report native amide-directed C(sp³)-H alkynylation reactions using an electron-deficient iridium catalyst and an electron-deficient pyridone ligand. Under the optimized conditions, the C(sp³)-H alkynylation of terminal methyl groups and internal methylene groups of cyclobutane carboxamides afforded the desired products in moderate to good yields.
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Kimura et al. (2025) studied this question.
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