cis-Selective Direct Halocyclopropanation of Alkenes Mediated by Nucleophilic Cobalt Photocatalysis

04 November 2025, Version 1
This content is an early or alternative research output and has not been peer-reviewed by Cambridge University Press at the time of posting.

Abstract

The cyclopropyl group is an invaluable motif in both medicinal and synthetic chemistry, with 1,2-disubstituted halocyclopropanes serving as important building blocks for the preparation of more complex cyclopropane-containing structures. Herein, we report a Vitamin B12-photocatalyzed approach for the direct synthesis of 1,2-disubstituted halocyclopropanes starting from alkenes and simple haloforms under visible-light irradiation. Our method yields a diverse range of 1,2-disubstituted halocyclopropanes with high cis-selectivity, providing efficient access to these traditionally difficult to prepare stereoisomers. Mechanistic studies highlight the crucial role of Vitamin B12 in influencing the stereochemical outcome of the reaction.

Keywords

Cyclopropanation
Stereoselective
Cobalt
Haloforms

Supplementary materials

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Description
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Supporting Information
Description
Experimental procedures, reaction optimization, compound characterization, and NMR spectra
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