Photoinduced Radical-Polar Crossover Enabling Three-Component Carbooxygenation of Arylalkenes

An efficient photoinduced radical-polar crossover strategy is described for the three-component carbooxygenation of arylalkenes, enabling their concomitant cyanomethylation/carbonylmethylation and esterification. This method facilitates the direct incorporation of cyanomethyl/carbonylmethyl and ester groups into readily available olefins using α-bromo nitriles/α-bromo esters and carboxylic acids as key reagents. The reaction proceeds under mild conditions at room temperature, exhibiting good functional group tolerance, a broad substrate scope, and high atom economy. Notably, despite the relatively weak nucleophilicity of carboxylic acids, they can be directly incorporated into this photoinduced radical-polar crossover transformation. Moreover, this protocol is also applicable to other nucleophiles, including alcohols, water, and aromatic amines, thereby significantly enhancing its synthetic versatility. This work offers a practical and versatile approach to constructing multifunctionalized molecules.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2026-04-17
DOI
https://doi.org/10.1021/acs.joc.6c00343
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Photoinduced Radical-Polar Crossover Enabling Three-Component Carbooxygenation of Arylalkenes

Zhu‐Ming Qian, Sheng-Ping Liu, Zhi Guan, Ming-Lin Yang et al.
The Journal of Organic Chemistry
Radical Photochemical Reactions
article

Photoinduced Radical-Polar Crossover Enabling Three-Component Carbooxygenation of Arylalkenes

Zhu‐Ming Qian, Sheng-Ping Liu, Zhi Guan, Ming-Lin Yang, Qin Zhang, Hong-Yin Cheng, Yan-Hong He
article en

Abstract

An efficient photoinduced radical-polar crossover strategy is described for the three-component carbooxygenation of arylalkenes, enabling their concomitant cyanomethylation/carbonylmethylation and esterification. This method facilitates the direct incorporation of cyanomethyl/carbonylmethyl and ester groups into readily available olefins using α-bromo nitriles/α-bromo esters and carboxylic acids as key reagents. The reaction proceeds under mild conditions at room temperature, exhibiting good functional group tolerance, a broad substrate scope, and high atom economy. Notably, despite the relatively weak nucleophilicity of carboxylic acids, they can be directly incorporated into this photoinduced radical-polar crossover transformation. Moreover, this protocol is also applicable to other nucleophiles, including alcohols, water, and aromatic amines, thereby significantly enhancing its synthetic versatility. This work offers a practical and versatile approach to constructing multifunctionalized molecules.

The Journal of Organic ChemistryVol. 91(17)
Southwest University (CN), Chongqing Municipal Government (CN)
National Natural Science Foundation of China, Southwest University
Openalex Percentile: Top 23%
Radical Photochemical Reactions
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