Iron-Catalyzed Photoredox Decarboxylative Hydroalkylation with Alkynes and Alkenes

A photocatalyzed decarboxylative hydroalkylation approach has been developed, providing efficient and stereoselective access to synthetically challenging <i>Z</i>-configured allylamine derivatives from carboxylic acids and alkynes. The reaction is mediated by an iron catalyst, offering a green, environmentally benign, and highly atom-economical process. Moreover, this protocol can be extended to the reaction with alkenes to furnish arylamines and aryl ethers. Overall, this strategy establishes a versatile synthetic platform for the functionalization of unsaturated hydrocarbons.

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Publication Details

Journal
Organic Letters
Published
2026-02-05
DOI
https://doi.org/10.1021/acs.orglett.5c05310
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
0.00
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article

Iron-Catalyzed Photoredox Decarboxylative Hydroalkylation with Alkynes and Alkenes

袁华堂, Rongqiang Li, Zhenzhu Hu, Jing Peng et al.
Organic Letters
Radical Photochemical Reactions
article

Iron-Catalyzed Photoredox Decarboxylative Hydroalkylation with Alkynes and Alkenes

袁华堂, Rongqiang Li, Zhenzhu Hu, Jing Peng, Yuxin Lin, Xiaoxiao Ma
article en

Abstract

A photocatalyzed decarboxylative hydroalkylation approach has been developed, providing efficient and stereoselective access to synthetically challenging <i>Z</i>-configured allylamine derivatives from carboxylic acids and alkynes. The reaction is mediated by an iron catalyst, offering a green, environmentally benign, and highly atom-economical process. Moreover, this protocol can be extended to the reaction with alkenes to furnish arylamines and aryl ethers. Overall, this strategy establishes a versatile synthetic platform for the functionalization of unsaturated hydrocarbons.

Organic LettersVol. 28(7)
Duke University (US), Huanghuai University (CN), Pharmaceutical Biotechnology (Czechia) (CZ)
Life in Land
Openalex Percentile: Top 63%
Radical Photochemical Reactions
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