Fe-electrocatalytic deoxygenative Giese reaction

A redox-neutral Fe-electrocatalytic deoxygenative Giese reaction is reported. Hydroxyl groups are among the most abundant functional groups, and thus, the development of efficient reactions for their conversion has significant importance in medicinal and process chemistry. Here, we present a redox-neutral Giese reaction via anodic oxidation to generate phosphonium ions in combination with a cathodic reduction to yield low-valent Fe-catalysts. This reaction represents a promising example of a redox-neutral reaction using an Fe-catalyst and electrochemistry. The results obtained in this study will facilitate the exploration of a wide range of novel reactions employing this redox cycle in the future.

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Publication Details

Journal
Nature Communications
Published
2025-09-26
DOI
https://doi.org/10.1038/s41467-025-63515-x
Citations
4
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
3.74

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article

Fe-electrocatalytic deoxygenative Giese reaction

Ken Yamazaki, Hugh Nakamura, Yuuya Nagata, Shangzhao Li et al.
4 citations
Nature Communications
Radical Photochemical Reactions
3.74
article

Fe-electrocatalytic deoxygenative Giese reaction

Ken Yamazaki, Hugh Nakamura, Yuuya Nagata, Shangzhao Li, Qing Chen, Longhui Yu, Hiroshige Ogawa, Yilin Ma
article en
4 citations

Abstract

A redox-neutral Fe-electrocatalytic deoxygenative Giese reaction is reported. Hydroxyl groups are among the most abundant functional groups, and thus, the development of efficient reactions for their conversion has significant importance in medicinal and process chemistry. Here, we present a redox-neutral Giese reaction via anodic oxidation to generate phosphonium ions in combination with a cathodic reduction to yield low-valent Fe-catalysts. This reaction represents a promising example of a redox-neutral reaction using an Fe-catalyst and electrochemistry. The results obtained in this study will facilitate the exploration of a wide range of novel reactions employing this redox cycle in the future.

Nature CommunicationsVol. 16(1)
Okayama University (JP), Hong Kong University of Science and Technology (HK), Hokkaido University (JP), National Institute for Materials Science (JP), University of Hong Kong (HK)
Hong Kong University of Science and Technology
Openalex Percentile: Top 7%
Radical Photochemical Reactions
3.74
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