Decarboxylative Borylation of Redox-Active Esters by Au/Amine Catalysis

Abstract This study reports the decarboxylative borylation of redox-active esters catalyzed by supported Au nanoparticles in combination with a catalytic amount of an amine. The supported Au catalyst mediates single-electron transfer from the amine to the redox-active ester, generating an alkyl radical that is subsequently trapped by a diboron reagent to afford the corresponding alkylboronate. The catalytic system tolerates a wide range of functional groups and the supported Au catalyst can be reused over multiple cycles.

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Publication Details

Journal
Chemistry Letters
Published
2026-09-19
DOI
https://doi.org/10.1093/chemle/upag190
Primary Topic
Organoboron and organosilicon chemistry
Type
article
Field-Weighted Citation Impact
0.00
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article

Decarboxylative Borylation of Redox-Active Esters by Au/Amine Catalysis

Hiroki Miura, Tetsuya Shishido, Yushi Sato
Chemistry Letters
Organoboron and organosilicon chemistry
article

Decarboxylative Borylation of Redox-Active Esters by Au/Amine Catalysis

Hiroki Miura, Tetsuya Shishido, Yushi Sato
article en

Abstract

Abstract This study reports the decarboxylative borylation of redox-active esters catalyzed by supported Au nanoparticles in combination with a catalytic amount of an amine. The supported Au catalyst mediates single-electron transfer from the amine to the redox-active ester, generating an alkyl radical that is subsequently trapped by a diboron reagent to afford the corresponding alkylboronate. The catalytic system tolerates a wide range of functional groups and the supported Au catalyst can be reused over multiple cycles.

Chemistry Letters
Institute for Molecular Science (JP), Tokyo Metropolitan University (JP)
Clean water and sanitation
Openalex Percentile: Top 20%
Organoboron and organosilicon chemistry
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