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Aziridines — three-membered nitrogen-containing heterocycles — are important synthetic targets, but _N_-alkyl aziridines are difficult to synthesize. Now, an electrochemical method,
involving a dicationic intermediate, enables the coupling of alkenes and amines. Access through your institution Buy or subscribe This is a preview of subscription content, access via your
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subscriptions * Read our FAQs * Contact customer support REFERENCES * Gabriel, S. _Chem. Ber._ 21, 1049–1057 (1888). Article Google Scholar * Sweeney, J. B. _Chem. Soc. Rev._ 31, 247–258
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Merck & Co., Inc., Rahway, NJ, USA Tiffany Piou & Louis-Charles Campeau Authors * Tiffany Piou View author publications You can also search for this author inPubMed Google Scholar *
Louis-Charles Campeau View author publications You can also search for this author inPubMed Google Scholar CORRESPONDING AUTHOR Correspondence to Louis-Charles Campeau. ETHICS DECLARATIONS
COMPETING INTERESTS The authors declare no competing interests. RIGHTS AND PERMISSIONS Reprints and permissions ABOUT THIS ARTICLE CITE THIS ARTICLE Piou, T., Campeau, LC. Bringing amines
back into aziridination. _Nat. Chem._ 13, 1027–1028 (2021). https://doi.org/10.1038/s41557-021-00819-7 Download citation * Published: 25 October 2021 * Issue Date: November 2021 * DOI:
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