Electrochemical Biomimetic Iron‐Catalyzed Benzylic C─H Bonds Hydroxylation
Electrochemical synthesis has attracted considerable attention as a green synthetic technology in recent years, particularly in the domain of selective oxidation and reduction, which represents a significant yet ongoing challenge in the field. This protocol presents a biomimetic iron-catalyzed electrochemical benzylic C─H bond hydroxylation through a water activation strategy, where in situ-generated high-valent iron-oxo species mediate, enabling efficient and highly selective benzylic hydroxylation. The method exhibits excellent selectivity and broad functional group compatibility, applicable to primary, secondary, and tertiary benzylic C─H bonds, and suitable for late-stage modification of bioactive molecules. Mechanistic studies highlight the efficacy of a dual-control approach combining indirect electrolysis with a detached reaction layer to prevent direct substrate oxidation. This method offers a practical and green route to the synthesis of diverse benzyl alcohols.
Authors
- Chong Gao (ORCID: https://orcid.org/0000-0001-7639-0808)
- Jianhua Zhang (ORCID: https://orcid.org/0000-0001-7844-6035)
- Wentao Zhang (ORCID: https://orcid.org/0009-0006-8327-4171)
- Youai Qiu
- Min Liu
Institutions
- Nankai University (CN)
- State Key Laboratory of Chemical Engineering (CN)
- Zhejiang University of Technology (CN)
- Nanjing University (CN)
Publication Details
- Journal
- Angewandte Chemie International Edition
- Published
- 2026-04-13
- DOI
- https://doi.org/10.1002/anie.9980873
- Primary Topic
- Radical Photochemical Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Natural Science Foundation of China
- Natural Science Foundation of Tianjin City
- National Key Research and Development Program of China
- Fundamental Research Funds for the Central Universities