Nickel-Catalyzed Reductive Cyanation of Aryl Halides and Epoxides with Cyanogen Bromide.

Yu-Juan Wu, Chen Ma, Muhammad Bilal, Yu-Feng Liang

Abstract read

In one paragraph

Article in Molecules (Basel, Switzerland), 2024. 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.

Nickel-Catalyzed Cyanation of Aryl Halides.Molecules (Basel, Switzerland) · 2025
Review

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

4 authors.

Yu-Juan WuSchool of Chemistry and Chemical Engineering, Shandong University, Jinan 250100, China.

Chen MaSchool of Chemistry and Chemical Engineering, Shandong University, Jinan 250100, China.

Muhammad BilalSchool of Chemistry and Chemical Engineering, Shandong University, Jinan 250100, China.ORCID 0000-0002-8787-1399

Yu-Feng LiangSchool of Chemistry and Chemical Engineering, Shandong University, Jinan 250100, China.ORCID 0000-0002-9920-741X

Funding

Distinguished Young Scholars of Shandong Province (Overseas) 2022HWYQ-001National Natural Science Foundation of China 22001147Taishan Scholars Project of Shandong Province tsqn202103027

6 · The paper itself

Abstract

Nitriles are valuable compounds because they have widespread applications in organic chemistry. This report details the nickel-catalyzed reductive cyanation of aryl halides and epoxides with cyanogen bromide for the synthesis of nitriles. This robust protocol underscores the practicality of using a commercially available and cost-effective cyanation reagent. A variety of aryl halides and epoxides featuring diverse functional groups, such as -TMS, -Bpin, -OH, -NH

Indexed as

cyanationcyanogen bromidenickel catalysisnitrilesreductive coupling

Identifiers

PMID39770100

DOI10.3390/molecules29246016

PMCPMC11678332

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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.