Evidence map›Paper›PMID 41889779›Full record

ArticleJACS Au2026

Nickel-Catalyzed α‑Arylation and Alkenylation of α‑Trifluoromethyl Amines via 1,2-HAT Assisted by DMSO.

Muhammad Bilal, Kiran Fatima, Yu-Juan Wu, Yu-Qiu Guan, Yu-Feng Liang

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. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

5 authors.

Muhammad BilalSchool of Chemistry and Chemical Engineering, Shandong University, Jinan 250100, China.ORCID https://orcid.org/0000-0002-8787-1399
Kiran FatimaDepartment of Chemistry, Southern University of Science and Technology, Shenzhen 518055, China.
Yu-Juan WuSchool of Chemistry and Chemical Engineering, Shandong University, Jinan 250100, China.
Yu-Qiu GuanSchool of Chemistry and Chemical Engineering, Shandong University, Jinan 250100, China.
Yu-Feng LiangSchool of Chemistry and Chemical Engineering, Shandong University, Jinan 250100, China.ORCID https://orcid.org/0000-0002-9920-741X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

α-Trifluoromethyl amines are privileged scaffolds in pharmaceuticals and bioactive compounds, serving as metabolically stable amide bioisosteres. However, conventional synthetic approaches often suffer from multistep reactions, limited functional group tolerance, and instability of imine precursors. To overcome these limitations, we report a nickel-catalyzed cross-electrophilic coupling constructing diverse α-trifluoromethylamines via a mechanistically distinct pathway involving solvent-enabled 1,2-hydrogen atom transfer (HAT). In this process, the N-O bond is activated by Ni

Indexed as

1,2-hydrogen atom transfercross-electrophile couplingnickel catalysisradicalα-trifluoromethyl amines

Identifiers

PMID41889779
PMCPMC13014247

What OpenQuestion holds

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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.