Evidence map›Paper›PMID 42358692›Full record

ArticleJACS Au2026

John Hayford G Teye-Kau, Martin Pauze, Spencer P Pitre

Abstract read
In one paragraph

Article in JACS Au, 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.

John Hayford G Teye-KauDepartment of Chemistry, Oklahoma State University, Stillwater, Oklahoma 74078, United States.
Martin PauzeDepartment of Chemistry, Oklahoma State University, Stillwater, Oklahoma 74078, United States.ORCID https://orcid.org/0000-0002-9997-5662
Spencer P PitreDepartment of Chemistry, Oklahoma State University, Stillwater, Oklahoma 74078, United States.

Funding

Nucleophilic Cobalt Photocatalysis and Organic Single-Electron Photoreductants; Two Enabling Approaches for Chemical SynthesisR35GM154751 · NIGMS · OKLAHOMA STATE UNIVERSITY STILLWATER · PI Spencer Pitre · 2024 to 2026
$1.1M
NIGMS NIH HHS R35 GM154751
6 · The paper itself

Abstract

The cyclopropyl group is an invaluable motif in both medicinal and synthetic chemistry, with 1,2-disubstituted halocyclopropanes serving as important building blocks for the preparation of more complex cyclopropane-containing structures. Herein, we report a Vitamin B

Indexed as

alkenescis-selectivitycyclopropaneshaloformsvitamin B12

Identifiers

PMID42358692
PMCPMC13291968

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.