Catalyst‐Free and Visible Light‐Promoted Perfluoroalkylation of Indoles

ABSTRACT In this study, we report a catalyst‐free and photoinduced strategy for the direct perfluoroalkylation of heterocyclic indoles. This method demonstrates synthetic simplicity, mild reaction conditions, and eliminates the need for any catalyst, yielding perfluoroalkylated products in moderate to excellent yields. A diverse range of substrates, including various biologically relevant molecules, exhibited excellent compatibility with the reaction system, highlighting its potential for late‐stage functionalization of pharmaceutical analogues.

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Publication Details

Journal
Journal of Heterocyclic Chemistry
Published
2025-12-18
DOI
https://doi.org/10.1002/jhet.70154
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
0.00
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article

Catalyst‐Free and Visible Light‐Promoted Perfluoroalkylation of Indoles

Xun Sun, Xiaojing Su, Jing Wang, Lin Yin et al.
Journal of Heterocyclic Chemistry
Fluorine in Organic Chemistry
article

Catalyst‐Free and Visible Light‐Promoted Perfluoroalkylation of Indoles

Xun Sun, Xiaojing Su, Jing Wang, Lin Yin, J. H. Zou, Fan Zhou
article en

Abstract

ABSTRACT In this study, we report a catalyst‐free and photoinduced strategy for the direct perfluoroalkylation of heterocyclic indoles. This method demonstrates synthetic simplicity, mild reaction conditions, and eliminates the need for any catalyst, yielding perfluoroalkylated products in moderate to excellent yields. A diverse range of substrates, including various biologically relevant molecules, exhibited excellent compatibility with the reaction system, highlighting its potential for late‐stage functionalization of pharmaceutical analogues.

Journal of Heterocyclic ChemistryVol. 63(3)
Zunyi Medical University (CN), Kaili University (CN)
Openalex Percentile: Top 66%
Fluorine in Organic Chemistry
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