Synthesis of novel nucleophilic fluorinating reagents derived from KF

Clicks: 1
ID: 315349
2026
Free PDF
Article Quality & Performance Metrics
Overall Quality
Not rated
Combines reader engagement with the AI quality analysis. This article has not been analysed, so there is no overall score — reader engagement is measured and shown alongside.
AI Quality Assessment
Not analyzed
Readership in this journal

Ranked #767 of 788 articles by views in phytochemistry letters

Most read Least read

Bar heights use a square-root scale. Only the 120 most-read articles are drawn; the journal has 788 in total.

Mint this article as an NFT
Not yet minted

Create a permanent, verifiable on-chain record of this article on the Scimatic Network. The NFT is held in your Journament account, and you can withdraw it to your own wallet at any time.

5 SUSD one-off · no wallet required
Sign in to mint
Abstract
Abstract We present safe, convenient methods for synthesizing nucleophilic fluorinating reagents—specifically amine-3HF and R4NF(HFIP)3 complexes—using KF as a sustainable fluorine source. Cation exchange between KF and Amberlyst 15DRY generates HF in situ, enabling the efficient synthesis of various amine-3HF complexes. Alternatively, ion exchange between KF and R4NBr in an HFIP/CH2Cl2 co-solvent system provides a straightforward route to R4NF(HFIP)3 complexes. This review outlines the theoretical background, synthetic strategies, achievements, and future prospects of these KF-derived reagents.
Reference Key
openalex_W7162847476 Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Haruka Homma, Toshiki Tajima
Journal phytochemistry letters
Year 2026
DOI
10.1093/chemle/upag105
URL
https://doi.org/10.1093/chemle/upag105
Keywords Keywords not found

Citations

No citations found. To add a citation, contact the admin at info@scimatic.org

Comments

No comments yet. Be the first to comment on this article.