ArticleOrganic letters2014
Copper-catalyzed [18F]fluorination of (mesityl)(aryl)iodonium salts.
Article in Organic letters, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 86 papers.
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Who cites it
86 citing papers in PubMed.
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- Distinct hydrogen atom transfer and radical capture reactivity of copper(iii) OH/F complexes enables site-selective C(spChemical science · 2026Article
- PET and SPECT Tracer Development via Copper-Mediated Radiohalogenation of Divergent and Stable Aryl-Boronic Esters.Pharmaceutics · 2025Article
- Copper-mediated radiochemistry: historical impact, current trends, and future possibilities.Npj imaging · 2025Review
- Tandem Iridium-Catalyzed C-H Borylation/Copper-Mediated Radiofluorination of Aromatic C-H Bonds with [Methods in molecular biology (Clifton, N.J.) · 2024Article
- Preparation ofPharmaceutics · 2023Article
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- Radiochemistry for positron emission tomography.Nature communications · 2023Review
- Broad-scope Syntheses of [Chemistry (Weinheim an der Bergstrasse, Germany) · 2023Article
- One-Pot Radiosynthesis of [Molecules (Basel, Switzerland) · 2023Article
- Next Generation Copper Mediators for the Efficient Production ofChemistry (Weinheim an der Bergstrasse, Germany) · 2023Article
- Fully automatedScientific reports · 2022Article
- Recent Advances inPharmaceutics · 2022Review
- Isotopic Radiolabeling of the Antiretroviral Drug [Pharmaceuticals (Basel, Switzerland) · 2022Article
- Nucleophilic Radiofluorination Using Tri-Molecules (Basel, Switzerland) · 2022Article
- Arene radiofluorination enabled by photoredox-mediated halide interconversion.Nature chemistry · 2022Article
26 more citing papers are in PubMed but not listed here.
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Authors and funding
6 authors.
Funding
Abstract
A practical, rapid, and highly regioselective Cu-catalyzed radiofluorination of (mesityl)(aryl)iodonium salts is described. This protocol utilizes [(18)F]KF to access (18)F-labeled electron-rich, -neutral, and -deficient aryl fluorides under a single set of mild conditions. This methodology is applied to the synthesis of protected versions of two important radiotracers: 4-[(18)F]fluorophenylalanine and 6-[(18)F]fluoroDOPA.
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