Photoredox radical/polar crossover enables carbo-heterofunctionalization of alkenes: facile access to 1,3-difunctionalized nitro compounds
Herein, we present an efficient and practical method for multicomponent carbo-heterofunctionalization of alkenes <i>via</i> radical-polar crossover photoredox catalysis. Employing geminal bromonitroalkanes as redox-active reagents with a wide range of O-centered nucleophiles allows rapid access to various 1,3-difunctionalized nitro compounds, including β-nitro ketones, 1,3-nitro alcohols, 1,3-nitro ethers as well as cyclic molecules.
Authors
- Vasiliki Valsamidou
- Dmitry Katayev (ORCID: https://orcid.org/0000-0003-0131-1188)
- Bhargav N. Nandasana
- Subrata Patra (ORCID: https://orcid.org/0000-0003-3326-6713)
Institutions
- University of Bern (CH)
Publication Details
- Journal
- Chemical Communications
- Published
- 2024-12-20
- DOI
- https://doi.org/10.1039/d4cc06005a
- Citations
- 6
- Primary Topic
- Radical Photochemical Reactions
- Type
- article
- Field-Weighted Citation Impact
- 1.50