Iodine-Catalyzed Carbonyl-Alkyne Metathesis Reactions.

The reaction between aldehydes or ketones and alkynes-the carbonyl-alkyne metathesis-constitutes a very useful strategy for the synthesis of α,β-unsaturated carbonyls. We now demonstrate that iodine is a highly efficient catalyst for both the intra- and intermolecular metathesis reaction in very small concentrations (0.1-1 mol %). Our protocol outperforms other catalytic systems, is operationally very simple, cheap, metal-free, and tolerates a large variety of functional groups (e. g., -CN, -CO2Me, -Br, -OH) at very low catalyst loadings. We can furthermore show that iodine-catalyzed carbonyl-alkyne metatheses can be combined with other iodine-catalyzed reactions in one-pot procedures to afford larger and more complex molecular structures. Finally, our mechanistic studies indicate that the iodonium ion is the active catalyst under the reaction conditions.