Photoinduced radical addition of 4-alkyl-1,4-DHPs to vinyl azides
An efficient and operationally simple protocol for the synthesis of ketones <i>via</i> photoinduced radical addition of 4-alkyl-1,4-dihydropyridines (1,4-DHPs) to vinyl azides is described. The reaction proceeds under blue light irradiation, demonstrating broad functional group tolerance and moderate to excellent yields across a range of substrates. Mechanistic studies, including radical-trapping experiments, light on/off control experiments, and detailed Hammett analysis, substantiate a radical pathway. The use of dual-parameter Hammett correlations (<i>σ</i><sub>mb</sub> and <i>σ</i><sub>JJ˙</sub>) provides strong evidence for a radical pathway and elucidates key kinetic features of the transformation. This work delivers both a practical synthetic method and a fundamental mechanistic understanding of this radical addition reaction.
Authors
- Hongguang Du (ORCID: https://orcid.org/0000-0003-3237-4261)
- Jiajing Tan (ORCID: https://orcid.org/0000-0003-3825-9344)
- Zhiqin Zhang (ORCID: https://orcid.org/0000-0003-2127-6404)
- Ning Chen (ORCID: https://orcid.org/0000-0001-6660-4892)
- Xirui Zhang (ORCID: https://orcid.org/0000-0002-3081-3753)
Institutions
- Beijing University of Chemical Technology (CN)
Publication Details
- Journal
- Organic & Biomolecular Chemistry
- Published
- 2025-12-17
- DOI
- https://doi.org/10.1039/d5ob01647a
- Primary Topic
- Radical Photochemical Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.00