Evidence map›Paper›PMID 40871592›Full record

ReviewMolecules (Basel, Switzerland)2025

Nickel-Catalyzed Cyanation of Aryl Halides.

Zhenqiang Ma, Cuimeng Huo, Duo Zhou, Jingyi Zhang, Hongjun Kong, Wenke Ren, Fengbo Qu, Tingting Liu, Hui Chen, Xilong Wang

Abstract readReview
PubMed Full text at PMC Publisher
In one paragraph

Review in Molecules (Basel, Switzerland), 2025. 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

10 authors.

Zhenqiang MaHenan Province Key Laboratory of Environmentally Friendly Functional Materials, Institute of Chemistry, Henan Academy of Sciences, Zhengzhou 450002, China.
Cuimeng HuoHenan Province Key Laboratory of Environmentally Friendly Functional Materials, Institute of Chemistry, Henan Academy of Sciences, Zhengzhou 450002, China.
Duo ZhouHenan Province Key Laboratory of Environmentally Friendly Functional Materials, Institute of Chemistry, Henan Academy of Sciences, Zhengzhou 450002, China.
Jingyi ZhangHenan Province Key Laboratory of Environmentally Friendly Functional Materials, Institute of Chemistry, Henan Academy of Sciences, Zhengzhou 450002, China.
Hongjun KongHenan Province Key Laboratory of Environmentally Friendly Functional Materials, Institute of Chemistry, Henan Academy of Sciences, Zhengzhou 450002, China.
Wenke RenHenan Province Key Laboratory of Environmentally Friendly Functional Materials, Institute of Chemistry, Henan Academy of Sciences, Zhengzhou 450002, China.
Fengbo QuHenan Province Key Laboratory of Environmentally Friendly Functional Materials, Institute of Chemistry, Henan Academy of Sciences, Zhengzhou 450002, China.
Tingting LiuHenan Province Key Laboratory of Environmentally Friendly Functional Materials, Institute of Chemistry, Henan Academy of Sciences, Zhengzhou 450002, China.ORCID 0000-0002-0156-3054
Hui ChenHenan Province Key Laboratory of Environmentally Friendly Functional Materials, Institute of Chemistry, Henan Academy of Sciences, Zhengzhou 450002, China.
Xilong WangHenan Province Key Laboratory of Environmentally Friendly Functional Materials, Institute of Chemistry, Henan Academy of Sciences, Zhengzhou 450002, China.

Funding

he Fundamental Research Fund of Henan Academy of Sciences 20250603003The Henan Academy of Sciences Special Research Project 220503002the Joint Fund of Henan Province Science and Technology R&D Program 225200810059the Young Elite Scientists Sponsorship Program by the Henan Association for Science and Tech-nology 2025HYTP006
6 · The paper itself

Abstract

Nickel-catalyzed cyanation of aryl halides has emerged as a powerful and sustainable method for the synthesis of aryl nitriles-valuable motifs widely found in pharmaceuticals, agrochemicals, and functional materials. Compared to traditional cyanation methods that involve harsh conditions and toxic reagents, nickel catalysis enables mild, efficient, and versatile transformations. This review systematically summarizes recent advances in this field, categorized by different cyanide sources, including metal cyanides (NaCN, KCN, Zn(CN)

Indexed as

aryl halidescyanationnickel catalysis

Identifiers

PMID40871592
PMCPMC12388440

What Socratic 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 Socratic graph.