Organophotocatalytic Decarboxylative Allylation of Carboxylic Acids with Allylic Acetates

We developed an acridine-catalyzed, metal- and base-free decarboxylative allylation of carboxylic acids with allylic acetates under mild conditions. The reaction proceeds via a proton-coupled electron transfer (PCET) process, enabling efficient conversion of readily available feedstocks with broad functional group compatibility. This operationally simple and versatile method demonstrates significant potential for synthetic applications, particularly in late-stage modification of bioactive carboxylic acids.

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Publication Details

Journal
Organic Letters
Published
2025-09-26
DOI
https://doi.org/10.1021/acs.orglett.5c03690
Citations
4
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
3.74
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article

Organophotocatalytic Decarboxylative Allylation of Carboxylic Acids with Allylic Acetates

Teck‐Peng Loh, Yanzhe Shi, Yinlei Zhang, Xiaoyu Liu et al.
4 citations
Organic Letters
Radical Photochemical Reactions
3.74
article

Organophotocatalytic Decarboxylative Allylation of Carboxylic Acids with Allylic Acetates

Teck‐Peng Loh, Yanzhe Shi, Yinlei Zhang, Xiaoyu Liu, Peizhong Xie, C. Ju
article en
4 citations

Abstract

We developed an acridine-catalyzed, metal- and base-free decarboxylative allylation of carboxylic acids with allylic acetates under mild conditions. The reaction proceeds via a proton-coupled electron transfer (PCET) process, enabling efficient conversion of readily available feedstocks with broad functional group compatibility. This operationally simple and versatile method demonstrates significant potential for synthetic applications, particularly in late-stage modification of bioactive carboxylic acids.

Organic LettersVol. 27(40)
Nanjing Tech University (CN), Nanyang Technological University (SG), Henan University of Technology (CN), Division of Chemistry (US)
Openalex Percentile: Top 7%
Radical Photochemical Reactions
3.74
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