Evidence map›Paper›PMID 41966114›Full record

ArticleJournal of the American Chemical Society2026

Rhodium-Catalyzed Desymmetric Addition of Boronic Acids to Malononitriles.

Minghao Zhang, Qihao Zhang, Junjie Cao, Jun Joelle Wang, Jianchun Wang, Zhongxing Huang

Abstract read
In one paragraph

Article in Journal of the American Chemical Society, 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

6 authors.

Minghao ZhangState Key Laboratory of Synthetic Chemistry, Shanghai Hong Kong Joint Laboratory in Chemical Synthesis, Department of Chemistry, The University of Hong Kong, Hong Kong, China.
Qihao ZhangState Key Laboratory of Synthetic Chemistry, Shanghai Hong Kong Joint Laboratory in Chemical Synthesis, Department of Chemistry, The University of Hong Kong, Hong Kong, China.
Junjie CaoShenzhen Grubbs Institute and Department of Chemistry, Guangming Advanced Research Institute, and Guangdong Provincial Key Laboratory of Catalysis, Southern University of Science and Technology, Shenzhen 518055, China.
Jun Joelle WangDepartment of Chemistry, Hong Kong Baptist University, Kowloon, Hong Kong, China.ORCID 0000-0001-9723-4054
Jianchun WangShenzhen Grubbs Institute and Department of Chemistry, Guangming Advanced Research Institute, and Guangdong Provincial Key Laboratory of Catalysis, Southern University of Science and Technology, Shenzhen 518055, China.ORCID 0000-0002-3998-8699
Zhongxing HuangState Key Laboratory of Synthetic Chemistry, Shanghai Hong Kong Joint Laboratory in Chemical Synthesis, Department of Chemistry, The University of Hong Kong, Hong Kong, China.ORCID 0000-0003-0196-3469

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Malononitrile is a privileged chemical feedstock for building complex nitrogen-containing molecules of interest. However, achieving high enantiocontrol in transformations of its derivatives is often challenging, as the spatial arrangement of the two linear nitriles impedes the chelative assistance commonly exploited in related multifunctionalized reactants. Here, we demonstrate a customized phosphoramidite ligand for a rhodium-catalyzed desymmetric addition of carbon nucleophiles to malononitriles. The chiral pocket, enclosed by a vaulted, chlorinated binaphthol skeleton and an iminostilbene motif, is proposed to restrict the C(

Identifiers

PMID41966114
PMCPMC13107447

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Registered trials

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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.