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.
Authors
- Zhu‐Ming Qian
- Sheng-Ping Liu
- Zhi Guan (ORCID: https://orcid.org/0000-0002-0369-6141)
- Ming-Lin Yang
- Qin Zhang
- Hong-Yin Cheng
- Yan-Hong He (ORCID: https://orcid.org/0000-0002-6405-285X)
Institutions
- Southwest University (CN)
- Chongqing Municipal Government (CN)
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
Funders
- National Natural Science Foundation of China
- Southwest University