Carbonyl swapping converts cyclic ketones to saturated heterocycles | Nature
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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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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