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Metathesis-active ligands enable a catalytic functional group metathesis between aroyl chlorides and aryl iodides


Current methods for functional group interconversion have, for the most part, relied on relatively strong driving forces which often require highly reactive reagents to generate irreversibly a desired product in high yield and selectivity. These approaches generally prevent the use of the same catalytic strategy to perform the reverse reaction. Here we describe a catalytic functional group metathesis approach to interconvert, under CO-free conditions, two synthetically important classes of electrophiles that are often employed in the preparation of pharmaceuticals and agrochemicals—aroyl chlorides (ArCOCl) and aryl iodides (ArI). Our reaction design relies on the implementation of a key reversible ligand C–P bond cleavage event, which enables a non-innocent, metathesis-active phosphine ligand to mediate a rapid aryl group transfer between the two different electrophiles. Beyond enabling a practical and safer approach to the interconversion of ArCOCl and ArI, this type of ligand non-innocence provides a blueprint for the development of a broad range of functional group metathesis reactions employing synthetically relevant aryl electrophiles.

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Fig. 1: Conceptual blueprint for the development of a functional group metathesis reaction.
Fig. 2: Mechanistic hypothesis and preliminary experiments.
Fig. 3: Experimental evidence for the proposed functional group metathesis mechanism based on metathesis-active ligands.


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We thank Z. K. Wickens (Harvard University) for a critical proofreading of this manuscript. Generous funding from the Max-Planck-Society, the Max-Planck-Institut für Kohlenforschung and LG Chem (fellowship to Y.H.L.) is acknowledged. We thank B. List for sharing analytical equipment, and our NMR spectroscopy, mass spectrometry and X-ray departments for technical assistance.

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Authors and Affiliations



Y.H.L. and B.M. conceived the project and prepared the manuscript. B.M. directed the work. Y.H.L. developed and studied the reaction experimentally. Both the authors analysed the data.

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Correspondence to Bill Morandi.

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Supplementary information

Supplementary information

Supplementary experimental details and compound characterization data

Crystallographic data

CIF for compound 70; CCDC reference: 1829364

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Lee, Y.H., Morandi, B. Metathesis-active ligands enable a catalytic functional group metathesis between aroyl chlorides and aryl iodides. Nature Chem 10, 1016–1022 (2018).

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