1,n-Metal Migrations Mediated by 3d Transition Metals

Abstract Remote functionalization of unactivated sites remains a major challenge in transition-metal-catalyzed synthesis. This short review summarizes recent advances in through-space 1,n-metal migration reactions mediated by 3d transition metals, including Cr, Fe, Co, Ni, and Cu. These transformations enable site-selective bond formation at otherwise inaccessible positions and offer sustainable alternatives to conventional cross-coupling strategies. Mechanistic aspects such as ligand-controlled migration, σ-bond metathesis, isotope-labeling studies, and computational insights are highlighted to illustrate how regio- and stereoselectivity are achieved. Collectively, 3d metal-mediated 1,n-migration reactions provide a versatile platform for remote functionalization and open new avenues for reaction design in modern organic synthesis.

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Publication Details

Journal
Synthesis
Published
2026-02-02
DOI
https://doi.org/10.1055/a-2802-6100
Primary Topic
Catalytic Cross-Coupling Reactions
Type
article
Field-Weighted Citation Impact
0.00
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article

1,n-Metal Migrations Mediated by 3d Transition Metals

Ryo Shintani, Ikuya Fujii
Synthesis
Catalytic Cross-Coupling Reactions
article

1,n-Metal Migrations Mediated by 3d Transition Metals

Ryo Shintani, Ikuya Fujii
article en

Abstract

Abstract Remote functionalization of unactivated sites remains a major challenge in transition-metal-catalyzed synthesis. This short review summarizes recent advances in through-space 1,n-metal migration reactions mediated by 3d transition metals, including Cr, Fe, Co, Ni, and Cu. These transformations enable site-selective bond formation at otherwise inaccessible positions and offer sustainable alternatives to conventional cross-coupling strategies. Mechanistic aspects such as ligand-controlled migration, σ-bond metathesis, isotope-labeling studies, and computational insights are highlighted to illustrate how regio- and stereoselectivity are achieved. Collectively, 3d metal-mediated 1,n-migration reactions provide a versatile platform for remote functionalization and open new avenues for reaction design in modern organic synthesis.

Synthesis
Toyo University (JP), The University of Osaka (JP)
Openalex Percentile: Top 68%
Catalytic Cross-Coupling Reactions
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