Copper‐Mediated C4─H Selective Fluoroalkoxylation of Indoles via a Transient Directing Group Strategy

Comprehensive Summary Fluoroalkoxylated heterocycles, such as indoles, holds significant importance in pharmaceuticals and biology. Herein, we report a copper‐mediated C4–H fluoroalkoxylation reaction of indoles via a transient directing group (TDG) strategy. This reaction exhibits excellent regioselectivity and broad functional group compatibility, offering a new approach for the synthesis of fluoroalkoxylated indoles. The reaction also represents an unprecedented example of 3d‐transition metal‐catalyzed C─H fluoroalkoxylation via a TDG strategy.

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Publication Details

Journal
Chinese Journal of Chemistry
Published
2025-10-07
DOI
https://doi.org/10.1002/cjoc.70310
Citations
3
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
2.37
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article

Copper‐Mediated C4─H Selective Fluoroalkoxylation of Indoles via a Transient Directing Group Strategy

Yanghui Zhang, Ming‐Shun Mei
3 citations
Chinese Journal of Chemistry
Fluorine in Organic Chemistry
2.37
article

Copper‐Mediated C4─H Selective Fluoroalkoxylation of Indoles via a Transient Directing Group Strategy

Yanghui Zhang, Ming‐Shun Mei
article en
3 citations

Abstract

Comprehensive Summary Fluoroalkoxylated heterocycles, such as indoles, holds significant importance in pharmaceuticals and biology. Herein, we report a copper‐mediated C4–H fluoroalkoxylation reaction of indoles via a transient directing group (TDG) strategy. This reaction exhibits excellent regioselectivity and broad functional group compatibility, offering a new approach for the synthesis of fluoroalkoxylated indoles. The reaction also represents an unprecedented example of 3d‐transition metal‐catalyzed C─H fluoroalkoxylation via a TDG strategy.

Chinese Journal of ChemistryVol. 43(24)
Tongji University (CN)
Openalex Percentile: Top 10%
Fluorine in Organic Chemistry
2.37
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