Photo-Stitching of Nitroalkanes via Cross-Denitrative Olefination
Despite their centrality in molecular design, stereodefined tri- and tetrasubstituted alkenes remain challenging to access, as most olefinations favor lower substitution and fail under sterically congested settings. Herein, we report the photoinduced cross-denitrative olefination of nitroalkanes to afford tri- and tetrasubstituted alkenes. Visible light excitation of in situ-generated nitronates promotes a photo-stitching event via denitrative cross-coupling of two nitroalkanes. The transformation tolerates a variety of functionalized nitroalkanes, including carbonyl- and heterocycle-containing substrates, complements metathesis and carbonyl olefination, and scales efficiently. Mechanistic studies support a photoinitiated and photopropagated nucleophilic-radical substitution and radical-chain elimination sequence in which nitronates function as photoreductants to generate radical-anion intermediates that undergo a subsequent photodriven β-elimination. These findings establish a previously inaccessible light-driven elimination process for radical-mediated olefination from readily available building blocks.
Authors
- Joshua K. Mitchell (ORCID: https://orcid.org/0000-0002-8093-6823)
- Marvin Parasram (ORCID: https://orcid.org/0000-0002-6052-0417)
- Joseph Bergen
- Ajay H. Bansode (ORCID: https://orcid.org/0009-0005-5489-872X)
- Shrey P. Desai (ORCID: https://orcid.org/0000-0001-7031-0926)
- Maxwell S. McLean
- Poulami Ghosh
- Alexandria Reyes
Institutions
- New York University (US)
Publication Details
- Journal
- Journal of the American Chemical Society
- Published
- 2026-07-16
- DOI
- https://doi.org/10.1021/jacs.6c06460
- Citations
- 1
- Primary Topic
- Radical Photochemical Reactions
- Type
- article
- Field-Weighted Citation Impact
- 3.98
Funders
- Camille and Henry Dreyfus Foundation
- Amgen
- New York University
- York University
- National Institutes of Health
- National Institute of General Medical Sciences