Photocatalytic Denitrative Homo- and Cross-Coupling of Nitroalkanes toward the Synthesis of Alkenes

High Resolution Image Download MS PowerPoint Slide Alkenes serve as fundamental motifs across natural products and synthetic molecules, yet efficient, mild, and versatile olefination strategies remain in demand. Nitroalkanes, renowned for their broad reactivity as nucleophiles or corresponding radicals, still offer untapped potential in photocatalysis. Here, we report a unified, photocatalyzed generation of α-nitroalkyl radicals via oxidation of simple, nonprefunctionalized nitronates, followed by addition to another nitronate (formal homo- or cross-coupling) and subsequent double denitration to furnish alkenes. This transformation leverages both the pro-nucleophilic and pro-electrophilic nature of nitroalkanes, challenging the classic McMurry -type coupling protocol. Moreover, the synthetic manifold is scalable and demonstrates its applicability by synthesizing medicinally relevant Combretastatin and lignan-type cores.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2026-07-16
DOI
https://doi.org/10.1021/jacs.6c06459
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Photocatalytic Denitrative Homo- and Cross-Coupling of Nitroalkanes toward the Synthesis of Alkenes

Oliver Reiser, Jonas Scholl, Michael Gruber, Hendrik Paps et al.
Journal of the American Chemical Society
Radical Photochemical Reactions
article

Photocatalytic Denitrative Homo- and Cross-Coupling of Nitroalkanes toward the Synthesis of Alkenes

Oliver Reiser, Jonas Scholl, Michael Gruber, Hendrik Paps, Mangish Ghosh, Zen Shimizu, Max Dietel
article en

Abstract

High Resolution Image Download MS PowerPoint Slide Alkenes serve as fundamental motifs across natural products and synthetic molecules, yet efficient, mild, and versatile olefination strategies remain in demand. Nitroalkanes, renowned for their broad reactivity as nucleophiles or corresponding radicals, still offer untapped potential in photocatalysis. Here, we report a unified, photocatalyzed generation of α-nitroalkyl radicals via oxidation of simple, nonprefunctionalized nitronates, followed by addition to another nitronate (formal homo- or cross-coupling) and subsequent double denitration to furnish alkenes. This transformation leverages both the pro-nucleophilic and pro-electrophilic nature of nitroalkanes, challenging the classic McMurry -type coupling protocol. Moreover, the synthetic manifold is scalable and demonstrates its applicability by synthesizing medicinally relevant Combretastatin and lignan-type cores.

Journal of the American Chemical Society
University Hospital Regensburg (DE), Institute of Organic Chemistry (HU), Deutsche Gesellschaft für Anästhesiologie und Intensivmedizin (DE), University of Regensburg (DE)
Deutsche Forschungsgemeinschaft, Universität Regensburg, Elitenetzwerk Bayern
Openalex Percentile: Top 16%
Radical Photochemical Reactions
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