Evidence map›Paper›PMID 32366048›Full record

ReviewMolecules (Basel, Switzerland)2020

Kitamura Electrophilic Fluorination Using HF as a Source of Fluorine.

Jianlin Han, Greg Butler, Hiroki Moriwaki, Hiroyuki Konno, Vadim A Soloshonok, Tsugio Kitamura

Abstract readReview
PubMed Full text at PMC Publisher
In one paragraph

Review in Molecules (Basel, Switzerland), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Non-Aqueous Binary and TernaryJournal of the American Chemical Society · 2025
    Article
  2. Review
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Jianlin HanJiangsu Co-Innovation Center of Efficient Processing and Utilization of Forest Resources, College of Chemical Engineering, Nanjing Forestry University, Nanjing 210037, Jiangsu, China.
Greg ButlerOakwood Chemical, Inc. 730 Columbia Hwy. N, Estill, SC 29918, USA.
Hiroki MoriwakiHamari Chemical Ltd., 1-4-29 Kunijima, Higashi-Yodogawa-ku, Osaka 533-0024, Japan.
Hiroyuki KonnoDepartment of Biological Engineering, Graduate School of Science and Engineering, Yamagata University, Yonezawa, Yamagata 992-8510, Japan.
Vadim A SoloshonokDepartment of Organic Chemistry I, Faculty of Chemistry, University of the Basque Country UPV/EHU, Paseo Manuel Lardizábal 3, 20018 San Sebastián, Spain.
Tsugio KitamuraDepartment of Chemistry and Applied Chemistry, Saga University, 1 Honjo-machi, Saga 840-8502, Japan.

Funding

National Natural Science Foundation of China 21761132021
6 · The paper itself

Abstract

This review article focused on the innovative procedure for electrophilic fluorination using HF and in situ generation of the required electrophilic species derived from hypervalent iodine compounds. The areas of synthetic application of this approach include fluorination of 1,3-dicarbonyl compounds, aryl-alkyl ketones, styrene derivatives, α,β-unsaturated ketones and alcohols, homoallyl amine and homoallyl alcohol derivatives, 3-butenoic acids and alkynes.

Indexed as

HalogenationAlcoholsCatalysisCyclizationFluoridesFluorineHydrofluoric AcidKetonesMolecular StructureStyreneAlcoholsFluoridesFluorineHydrofluoric AcidKetonesStyrenebioactive compoundselectrophilic fluorinationfluorination reagentshydrogen fluoridehypervalent iodine

Identifiers

PMID32366048
PMCPMC7248860

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.