Unlocking the Accessibility of Alkyl/Aryl Radicals from Boronic Acids through EDA Complex Photoactivation

Herein, we present an eco-conscious carbon-carbon coupling reaction using boronic acids as alkyl/aryl radical sources through C-B bond photoactivation by an EDA complex. This method is characterized by its simplicity and efficiency, eliminating the need for photosensitizers, transition-metal catalysts, additives, or prefunctionalized starting materials. The facile derivatization of synthesized products and the capacity for late-stage pharmaceutical modification highlight the versatility and broad applicability of this method. Mechanistic investigations have clarified the radical pathway, emphasizing the crucial role of the EDA complex in initiating the transformation. This strategy offers valuable inspiration for developing green carbon-carbon coupling methods via boronic acid activation and opens new avenues for complex-based EDA transformations.

Authors

Institutions

Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-10-29
DOI
https://doi.org/10.1021/acs.joc.5c01558
Citations
8
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
7.49
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Unlocking the Accessibility of Alkyl/Aryl Radicals from Boronic Acids through EDA Complex Photoactivation

Kai Zheng, Jiangang Mao, Hao Xu, Chao Shen et al.
8 citations
The Journal of Organic Chemistry
Radical Photochemical Reactions
7.49
article

Unlocking the Accessibility of Alkyl/Aryl Radicals from Boronic Acids through EDA Complex Photoactivation

Kai Zheng, Jiangang Mao, Hao Xu, Chao Shen, Chao Chen
article en
8 citations

Abstract

Herein, we present an eco-conscious carbon-carbon coupling reaction using boronic acids as alkyl/aryl radical sources through C-B bond photoactivation by an EDA complex. This method is characterized by its simplicity and efficiency, eliminating the need for photosensitizers, transition-metal catalysts, additives, or prefunctionalized starting materials. The facile derivatization of synthesized products and the capacity for late-stage pharmaceutical modification highlight the versatility and broad applicability of this method. Mechanistic investigations have clarified the radical pathway, emphasizing the crucial role of the EDA complex in initiating the transformation. This strategy offers valuable inspiration for developing green carbon-carbon coupling methods via boronic acid activation and opens new avenues for complex-based EDA transformations.

The Journal of Organic ChemistryVol. 90(44)
Institute of Molecular Functional Materials (CN), Zhejiang Shuren University (CN), Jiangxi University of Science and Technology (CN)
Openalex Percentile: Top 2%
Radical Photochemical Reactions
7.49
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.