Evidence map›Paper›PMID 42070074›Full record

ArticleAngewandte Chemie (International ed. in English)2026

Geminal Difunctionalization of Ketones via C─S Bond Insertion of Photogenerated Donor-Donor Diazo Compounds.

Vincent George, Aryaman Pattanaik, Daniel Maddox, Lukas M Sigmund, Giovanna Mejia, Sara Pahlén, Simon O Angerer, Maria Schmoll, Lisa Marie Schneider, Nidhal Selmi and 4 more

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 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

14 authors.

Vincent GeorgeFaculty of Chemistry and Pharmacy, University of Regensburg, Regensburg, Germany.
Aryaman PattanaikFaculty of Chemistry and Pharmacy, University of Regensburg, Regensburg, Germany.
Daniel MaddoxCompound Synthesis and Management, Discovery Sciences, BioPharmaceuticals R&D, AstraZeneca, Mölndal, Sweden.
Lukas M SigmundMolecular AI, Discovery Sciences, BioPharmaceuticals R&D, AstraZeneca, Mölndal, Sweden.
Giovanna MejiaCompound Synthesis and Management, Discovery Sciences, BioPharmaceuticals R&D, AstraZeneca, Mölndal, Sweden.
Sara PahlénCompound Synthesis and Management, Discovery Sciences, BioPharmaceuticals R&D, AstraZeneca, Mölndal, Sweden.
Simon O AngererFaculty of Chemistry and Pharmacy, University of Regensburg, Regensburg, Germany.
Maria SchmollFaculty of Chemistry and Pharmacy, University of Regensburg, Regensburg, Germany.
Lisa Marie SchneiderFaculty of Chemistry and Pharmacy, University of Regensburg, Regensburg, Germany.
Nidhal SelmiCompound Synthesis and Management, Discovery Sciences, BioPharmaceuticals R&D, AstraZeneca, Mölndal, Sweden.
Mikhail KabeshovMolecular AI, Discovery Sciences, BioPharmaceuticals R&D, AstraZeneca, Mölndal, Sweden.
Giulia BergonziniCompound Synthesis and Management, Discovery Sciences, BioPharmaceuticals R&D, AstraZeneca, Mölndal, Sweden.
Julia RehbeinFaculty of Chemistry and Pharmacy, University of Regensburg, Regensburg, Germany.ORCID https://orcid.org/0000-0001-9241-0637
Burkhard KönigFaculty of Chemistry and Pharmacy, University of Regensburg, Regensburg, Germany.ORCID https://orcid.org/0000-0002-6131-4850

Funding

German Science Foundation 2620-426795949
6 · The paper itself

Abstract

Geminal difunctionalization of carbonyl-derived building blocks represents a versatile strategy for the rapid generation of sp

Indexed as

chemical librarydiazo compoundsdifunctionalizationflow chemistryphotochemistry

Identifiers

PMID42070074
PMCPMC13266950

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.