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.
Authors
- Oliver Reiser (ORCID: https://orcid.org/0000-0003-1430-573X)
- Jonas Scholl
- Michael Gruber (ORCID: https://orcid.org/0000-0002-5509-9760)
- Hendrik Paps
- Mangish Ghosh (ORCID: https://orcid.org/0009-0005-2632-303X)
- Zen Shimizu
- Max Dietel
Institutions
- University Hospital Regensburg (DE)
- Institute of Organic Chemistry (HU)
- Deutsche Gesellschaft für Anästhesiologie und Intensivmedizin (DE)
- University of Regensburg (DE)
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
Funders
- Deutsche Forschungsgemeinschaft
- Universität Regensburg
- Elitenetzwerk Bayern