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.
Authors
- Dandan Zhao (ORCID: https://orcid.org/0000-0001-5194-750X)
- Yanli Xu
- Hongyan Yang (ORCID: https://orcid.org/0000-0002-6809-5494)
- Peng He (ORCID: https://orcid.org/0000-0002-7141-4660)
- Xiaoli Wang (ORCID: https://orcid.org/0000-0003-3136-9807)
- Qifu Lin (ORCID: https://orcid.org/0000-0003-2669-4058)
Institutions
- Japan Advanced Institute of Science and Technology (JP)
- Beibu Gulf University (CN)
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
- Field-Weighted Citation Impact
- 0.00