<i>cis</i> -Selective Direct Halocyclopropanation of Alkenes Mediated by Nucleophilic Cobalt Photocatalysis

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.

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Publication Details

Journal
JACS Au
Published
2026-05-31
DOI
https://doi.org/10.1021/jacsau.6c00381
Primary Topic
Cyclopropane Reaction Mechanisms
Type
article
Field-Weighted Citation Impact
0.00
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article

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

John Hayford G. Teye‐Kau, Martin Pauze, Spencer P. Pitre
JACS Au
Cyclopropane Reaction Mechanisms
article

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

John Hayford G. Teye‐Kau, Martin Pauze, Spencer P. Pitre
article en

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.

JACS Au
Oklahoma State University Oklahoma City (US)
Openalex Percentile: Top 10%
Cyclopropane Reaction Mechanisms
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