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.

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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

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article

Photo-Stitching of Nitroalkanes via Cross-Denitrative Olefination

Joshua K. Mitchell, Marvin Parasram, Joseph Bergen, Ajay H. Bansode et al.
1 citations
Journal of the American Chemical Society
Radical Photochemical Reactions
3.98
article

Photo-Stitching of Nitroalkanes via Cross-Denitrative Olefination

Joshua K. Mitchell, Marvin Parasram, Joseph Bergen, Ajay H. Bansode, Shrey P. Desai, Maxwell S. McLean, Poulami Ghosh, Alexandria Reyes
article en
1 citations

Abstract

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.

Journal of the American Chemical Society
New York University (US)
Camille and Henry Dreyfus Foundation, Amgen, New York University, York University, National Institutes of Health, National Institute of General Medical Sciences
Openalex Percentile: Top 5%
Radical Photochemical Reactions
3.98
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