Photoredox/Nickel Dual-Catalyzed Asymmetric C-Alkylation of Nitroalkanes with α-Bromoketones

A stereoselective method for alkylating nitroalkanes with α-bromoketones using nickel/photoredox dual catalysis is described. The mild and functional-group-tolerant conditions allow the formation of complex and highly enantioenriched β-nitroketone products that hold promising utility as precursors for the formation of biologically relevant compounds.

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Publication Details

Journal
Organic Letters
Published
2025-12-08
DOI
https://doi.org/10.1021/acs.orglett.5c04507
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
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article

Photoredox/Nickel Dual-Catalyzed Asymmetric C-Alkylation of Nitroalkanes with α-Bromoketones

Raphael S. Kim, Donald A. Watson, Sina Rezazadeh
Organic Letters
Radical Photochemical Reactions
article

Photoredox/Nickel Dual-Catalyzed Asymmetric C-Alkylation of Nitroalkanes with α-Bromoketones

Raphael S. Kim, Donald A. Watson, Sina Rezazadeh
article en

Abstract

A stereoselective method for alkylating nitroalkanes with α-bromoketones using nickel/photoredox dual catalysis is described. The mild and functional-group-tolerant conditions allow the formation of complex and highly enantioenriched β-nitroketone products that hold promising utility as precursors for the formation of biologically relevant compounds.

Organic LettersVol. 28(2)
University of Delaware (US)
Openalex Percentile: Top 70%
Radical Photochemical Reactions
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Photoredox/Nickel Dual-Catalyzed Asymmetric C-Alkylation of Nitroalkanes with α-Bromoketones — Raphael S. Kim, Donald A. Watson, et al. · Organic Letters (2025) | TGRS Research Map | TGRS