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Carbonyl swapping converts cyclic ketones to saturated heterocycles | Nature

Source: NatureView Original
scienceApril 15, 2026

Subjects

- Synthetic chemistry methodology

Abstract

Saturated heterocycles are privileged scaffolds in bioactive molecules.1 Despite the availability of numerous de novo routes to various heterocyclic compounds, accessing diverse heterocycles from a unified, readily available carbocycle would offer a strategic alternative for constructing challenging heterocyclic structures from unconventional precursors.2 Here we report a modular approach that transforms a single cyclic ketone into various saturated heterocycles through formal carbonyl replacement with heteroatoms, via a scarcely explored bis(aroylperoxy) ketal intermediate. Through electronically guided peroxy cleavage, this intermediate enables double C–C bond scission of cyclic ketones, generating alkyl dichlorides as versatile handles for modular N/O/S/Se/Te incorporation using simple nucleophiles. This method exhibits broad substrate scope and functional-group tolerance, enabling both accelerated target synthesis and late-stage diversification of bioactive molecules. Its utility is also extended through “ring construction–carbonyl replacement” and “ring functionalization–carbonyl replacement” strategies, whereby cyclic ketones prepared via well-established methods are converted into challenging-to-access heterocycles for which analogous methods remain underdeveloped. By combining C–H oxidation with carbonyl replacement, a proof-of-concept formal “CH2-to-heteroatom” conversion is further demonstrated.

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Author information

Author notes- These authors contributed equally: Zisheng Xue, Zhengzhao Lou

Authors and Affiliations

- Beijing National Laboratory of Molecular Sciences, College of Chemistry and Molecular Engineering, Peking University, Beijing, China

Zisheng Xue, Zhengzhao Lou, Xiang Lou, Peimiao He, Jianbo Wang & Yan Xu

- Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, Peking University, Beijing, China

Zisheng Xue, Zhengzhao Lou, Xiang Lou, Peimiao He, Jianbo Wang & Yan Xu

- College of Chemistry and Chemical Engineering, Inner Mongolia University, Hohhot, China

Jianbo Wang

Authors- Zisheng XueView author publications

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- Zhengzhao LouView author publications

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- Xiang LouView author publications

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- Peimiao HeView author publications

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- Jianbo WangView author publications

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- Yan XuView author publications

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Corresponding author

Correspondence to

Yan Xu.

Supplementary information

Supplementary Information (download PDF )

This Supplementary Information file contains the following 10 sections: 1. General considerations; 2. Substrate synthesis; 3. Studies on bis(aroylperoxy) ketals and establishment of optimal protocols for CO-to-N swap; 4. Substrate scope of the CO-to-N swap; 5. Divergent transformation of cyclic ketones to heterocycles via modular CO-to-N/O/S/Se/Te swap; 6. Two-phase synthesis via CO-to-X swap: “ring construction–carbonyl replacement” and “ring functionalization–carbonyl replacement” strategies; 7. A proof-of-concept study on the formal CH2-to-X replacement; 8. Further study; 9. References; and 10. Spectra.

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Cite this article

Xue, Z., Lou, Z., Lou, X. et al. Carbonyl swapping converts cyclic ketones to saturated heterocycles.

Nature (2026). https://doi.org/10.1038/s41586-026-10508-5

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- Received: 16 December 2025

- Accepted: 08 April 2026

- Published: 15 April 2026

- DOI: https://doi.org/10.1038/s41586-026-10508-5

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