Deacylative Polyfluoroarylation via C–C Cleavage of Alkyl Ketones

Polyfluoroarenes often exist in functional molecules; however, construction of alkyl-polyfluoroaryl bonds remains nontrivial, and the current approaches exhibit various limitations. Here we report the first deacylative polyfluoroarylation of readily available methyl ketones, enabled by aromatization-driven C-C bond cleavage. This method allows efficient synthesis of both primary and secondary alkyl-substituted polyfluoroarenes under simple and convenient conditions, demonstrating excellent functional group tolerance and generality. The preliminary mechanistic study suggests the involvement of direct addition of the alkyl radical intermediate, generated after the C-C bond cleavage, to the polyfluoroarene, followed by either a single-electron transfer (SET) or hydrogen-atom transfer (HAT) process with the prearomatic intermediate (PAI).

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Publication Details

Journal
Organic Letters
Published
2025-09-22
DOI
https://doi.org/10.1021/acs.orglett.5c03436
Citations
1
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
0.79
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article

Deacylative Polyfluoroarylation via C–C Cleavage of Alkyl Ketones

Guangbin Dong, Ching‐Nung Chen, Scott A. Snyder, Sohee Kim
1 citations
Organic Letters
Fluorine in Organic Chemistry
0.79
article

Deacylative Polyfluoroarylation via C–C Cleavage of Alkyl Ketones

Guangbin Dong, Ching‐Nung Chen, Scott A. Snyder, Sohee Kim
article en
1 citations

Abstract

Polyfluoroarenes often exist in functional molecules; however, construction of alkyl-polyfluoroaryl bonds remains nontrivial, and the current approaches exhibit various limitations. Here we report the first deacylative polyfluoroarylation of readily available methyl ketones, enabled by aromatization-driven C-C bond cleavage. This method allows efficient synthesis of both primary and secondary alkyl-substituted polyfluoroarenes under simple and convenient conditions, demonstrating excellent functional group tolerance and generality. The preliminary mechanistic study suggests the involvement of direct addition of the alkyl radical intermediate, generated after the C-C bond cleavage, to the polyfluoroarene, followed by either a single-electron transfer (SET) or hydrogen-atom transfer (HAT) process with the prearomatic intermediate (PAI).

Organic LettersVol. 27(39)
University of Chicago (US)
Openalex Percentile: Top 23%
Fluorine in Organic Chemistry
0.79
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