Anti-Markovnikov Hydroacylation of Aryl Alkenes with Aldehydes Enabled by Photo/Cobalt Dual Catalysis

Herein we describe a dual photo/cobalt-catalyzed anti-Markovnikov hydroacylation of aryl alkenes using aldehyde as acyl source. The key to success is the cobalt catalyzed hydrogen atom transfer, which enables effective formation of the desired products and efficient regeneration of the photocatalyst under mild conditions. This protocol features broad substrate scopes, good functional group tolerance, high efficiency and regioselectivity.

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Publication Details

Journal
Organic Letters
Published
2024-12-28
DOI
https://doi.org/10.1021/acs.orglett.4c04373
Citations
4
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
1.00

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article

Anti-Markovnikov Hydroacylation of Aryl Alkenes with Aldehydes Enabled by Photo/Cobalt Dual Catalysis

Guanghao Ji, Xuan Li, J. Zhang
4 citations
Organic Letters
Sulfur-Based Synthesis Techniques
1.00
article

Anti-Markovnikov Hydroacylation of Aryl Alkenes with Aldehydes Enabled by Photo/Cobalt Dual Catalysis

Guanghao Ji, Xuan Li, J. Zhang
article en
4 citations

Abstract

Herein we describe a dual photo/cobalt-catalyzed anti-Markovnikov hydroacylation of aryl alkenes using aldehyde as acyl source. The key to success is the cobalt catalyzed hydrogen atom transfer, which enables effective formation of the desired products and efficient regeneration of the photocatalyst under mild conditions. This protocol features broad substrate scopes, good functional group tolerance, high efficiency and regioselectivity.

Organic LettersVol. 27(1)
Wuhan University (CN)
National Natural Science Foundation of China, Wuhan University, Fundamental Research Funds for the Central Universities
Openalex Percentile: Top 25%
Sulfur-Based Synthesis Techniques
1.00
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