Iridium‐Catalyzed <i>Anti</i> ‐Stereoselective Ring‐Opening Fluoroalkoxylation of Heterobicyclic Alkenes

ABSTRACT A highly efficient iridium‐catalyzed ring‐opening reactions of heterobicyclic alkenes with fluoroalkyl alcohols has been developed. The reaction utilizes readily available fluoroalkyl alcohols as fluoroalkoxylation reagents and exhibits a wide substrate scope, affording the fluoroalkoxylated products with trans ‐1,2‐disubstituted dihydronaphthalene framework in good to excellent yields. Mechanistic insights, supported by computational studies, have been proposed to elucidate the reaction pathway.

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Publication Details

Journal
Asian Journal of Organic Chemistry
Published
2025-11-30
DOI
https://doi.org/10.1002/ajoc.70274
Primary Topic
Fluorine in Organic Chemistry
Type
article
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article

Iridium‐Catalyzed Anti ‐Stereoselective Ring‐Opening Fluoroalkoxylation of Heterobicyclic Alkenes

Dandan Zhao, Yanli Xu, Hongyan Yang, Peng He et al.
Asian Journal of Organic Chemistry
Fluorine in Organic Chemistry
article

Iridium‐Catalyzed Anti ‐Stereoselective Ring‐Opening Fluoroalkoxylation of Heterobicyclic Alkenes

Dandan Zhao, Yanli Xu, Hongyan Yang, Peng He, Xiaoli Wang, Qifu Lin
article en

Abstract

ABSTRACT A highly efficient iridium‐catalyzed ring‐opening reactions of heterobicyclic alkenes with fluoroalkyl alcohols has been developed. The reaction utilizes readily available fluoroalkyl alcohols as fluoroalkoxylation reagents and exhibits a wide substrate scope, affording the fluoroalkoxylated products with trans ‐1,2‐disubstituted dihydronaphthalene framework in good to excellent yields. Mechanistic insights, supported by computational studies, have been proposed to elucidate the reaction pathway.

Asian Journal of Organic ChemistryVol. 15(1)
Japan Advanced Institute of Science and Technology (JP), Beibu Gulf University (CN)
Openalex Percentile: Top 69%
Fluorine in Organic Chemistry
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