Demonstrates the rapid synthesis of aryl heteroaryl ketones from aldehydes, suggesting a useful method for drug development.
The N-heterocyclic carbene (NHC)-catalyzed C-H heteroarylation of aromatic aldehydes for the synthesis of aryl heteroaryl ketones under mild and metal-free conditions is reported. This operationally simple strategy proceeds via the nucleophilic substitution of aldehyde-derived Breslow intermediates with 2-chloro-substituted heteroarenes in an addition-elimination pathway following the irreversible formation of benzoin. Moreover, the reaction exhibited good functional group tolerance, providing access to a diverse range of heteroaryl ketones in moderate to high yields. In addition, the synthetic utility of the method is demonstrated through the preparation of pharmaceutically relevant molecules.
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Mukhopadhyay et al. (2026) studied this question.
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