Evidence map›Paper›PMID 42774905›Full record

ArticleOrganic chemistry frontiers : an international journal of organic chemistry2026

A unified strategy for α-alkoxyalkyl radical generation

Emy André-Joyaux, Lise Benoist, Agathe Fayolle, Fabrice Dénès, Philippe Renaud

Abstract read
In one paragraph

Article in Organic chemistry frontiers : an international 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

5 authors.

Emy André-JoyauxUniversity of Bern, Department of Chemistry, Biochemistry and Pharmaceutical Sciences Freiestrasse 3 CH-3012 Bern Switzerland philippe.renaud@unibe.ch fabrice.denes@univ-nantes.fr.ORCID https://orcid.org/0000-0002-2239-2768
Lise BenoistUniversity of Bern, Department of Chemistry, Biochemistry and Pharmaceutical Sciences Freiestrasse 3 CH-3012 Bern Switzerland philippe.renaud@unibe.ch fabrice.denes@univ-nantes.fr.ORCID https://orcid.org/0009-0008-0458-0651
Agathe FayolleUniversity of Bern, Department of Chemistry, Biochemistry and Pharmaceutical Sciences Freiestrasse 3 CH-3012 Bern Switzerland philippe.renaud@unibe.ch fabrice.denes@univ-nantes.fr.
Fabrice DénèsUniversity of Bern, Department of Chemistry, Biochemistry and Pharmaceutical Sciences Freiestrasse 3 CH-3012 Bern Switzerland philippe.renaud@unibe.ch fabrice.denes@univ-nantes.fr.ORCID https://orcid.org/0000-0002-9791-3177
Philippe RenaudUniversity of Bern, Department of Chemistry, Biochemistry and Pharmaceutical Sciences Freiestrasse 3 CH-3012 Bern Switzerland philippe.renaud@unibe.ch fabrice.denes@univ-nantes.fr.ORCID https://orcid.org/0000-0002-9069-7109

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A general method to generate α-alkoxyalkyl radicals from pinacol boronic ester precursors (R-Bpin) has been developed. These radical precursors are stable in air, easy to prepare, and readily accessible

Identifiers

PMID42774905
PMCPMC13596088

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.