Evidence map›Paper›PMID 42290057›Full record

ArticleThe Journal of organic chemistry2026

Atypical Outcome of the Giese Reaction with Halogenated Enones.

Vojtěch Kundera, Judit E Šponer, Jakub Švenda

Abstract read
In one paragraph

Article in The Journal of organic chemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Vojtěch KunderaDepartment of Chemistry, Faculty of Science, Masaryk University, Kamenice 5, Brno 625 00, Czech Republic.ORCID 0009-0004-2568-0863
Judit E ŠponerInstitute of Biophysics of the Czech Academy of Sciences, Brno 612 65, Czech Republic.
Jakub ŠvendaDepartment of Chemistry, Faculty of Science, Masaryk University, Kamenice 5, Brno 625 00, Czech Republic.ORCID 0000-0001-9232-3218

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An atypical pathway in the Giese reaction is being reported. Photoredox-mediated 1,4-addition of α-amino radicals onto an α'-fluorinated enone was found to proceed with a loss of fluoride and retention of the acceptor C═C bond. Experimental observations and computational analysis are consistent with the initially formed fluorinated α-carbonyl radical intermediate undergoing rapid deprotonation rather than the typically observed one-electron reduction. This underexplored reactivity may aid the development of an oxidative Giese reaction.

Identifiers

PMID42290057
PMCPMC13316980

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Registered trials

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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.