Nickel/Photoredox‐Catalyzed Reductive Aldol Reaction

A dual nickel/photoredox‐catalyzed reductive aldol reaction using readily available alkyl bromide and α‐silylamine as bench‐stable hydride source and organic reductant is reported. A variety of β‐hydroxyl carbonyl compounds can be efficiently synthesized under mild conditions. The reaction exhibits broad substrate scope, accommodating various (hetero)aromatic and aliphatic aldehydes, as well as acyclic and cyclic α,β‐unsaturated carbonyls.

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Publication Details

Journal
Advanced Synthesis & Catalysis
Published
2025-10-26
DOI
https://doi.org/10.1002/adsc.70192
Primary Topic
Radical Photochemical Reactions
Type
article
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article

Nickel/Photoredox‐Catalyzed Reductive Aldol Reaction

Weiming Yuan, Wenlong Wang, Long Wang, Xianzhou Zheng
Advanced Synthesis & Catalysis
Radical Photochemical Reactions
article

Nickel/Photoredox‐Catalyzed Reductive Aldol Reaction

Weiming Yuan, Wenlong Wang, Long Wang, Xianzhou Zheng
article en

Abstract

A dual nickel/photoredox‐catalyzed reductive aldol reaction using readily available alkyl bromide and α‐silylamine as bench‐stable hydride source and organic reductant is reported. A variety of β‐hydroxyl carbonyl compounds can be efficiently synthesized under mild conditions. The reaction exhibits broad substrate scope, accommodating various (hetero)aromatic and aliphatic aldehydes, as well as acyclic and cyclic α,β‐unsaturated carbonyls.

Advanced Synthesis & CatalysisVol. 367(24)
Ministry of Education (RO), Wuhan National Laboratory for Optoelectronics (CN), Huazhong University of Science and Technology (CN)
Openalex Percentile: Top 77%
Radical Photochemical Reactions
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