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.

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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
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article

Photoredox radical/polar crossover enables carbo-heterofunctionalization of alkenes: facile access to 1,3-difunctionalized nitro compounds

Vasiliki Valsamidou, Dmitry Katayev, Bhargav N. Nandasana, Subrata Patra
6 citations
Chemical Communications
Radical Photochemical Reactions
1.50
article

Photoredox radical/polar crossover enables carbo-heterofunctionalization of alkenes: facile access to 1,3-difunctionalized nitro compounds

Vasiliki Valsamidou, Dmitry Katayev, Bhargav N. Nandasana, Subrata Patra
article en
6 citations

Abstract

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.

Chemical CommunicationsVol. 61(8)
University of Bern (CH)
Openalex Percentile: Top 18%
Radical Photochemical Reactions
1.50
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