Evidence map›Paper›PMID 42317674›Full record

ArticleChemical science2026

Organocatalytic asymmetric synthesis of atropisomeric tetraarylethenes: design, properties, and applications.

Mei An, Chuan-Jun Lu, Fei Xie, Yin-Jian Sun, Zhaofeng Sun, Long-Long Xi, Ren-Rong Liu

Abstract read
In one paragraph

Article in Chemical science, 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
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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

7 authors.

Mei AnCollege of Pharmaceutical Sciences, Guizhou University Guiyang Guizhou 550025 China renrongliu@qdu.edu.cn.
Chuan-Jun LuCollege of Chemistry and Chemical Engineering, Qingdao University Qingdao 266071 China xill@qdu.edu.cn.ORCID https://orcid.org/0000-0003-1116-7642
Fei XieCollege of Chemistry and Chemical Engineering, Qingdao University Qingdao 266071 China xill@qdu.edu.cn.
Yin-Jian SunCollege of Chemistry and Chemical Engineering, Qingdao University Qingdao 266071 China xill@qdu.edu.cn.ORCID https://orcid.org/0009-0002-8261-3945
Zhaofeng SunSchool of Rehabilitation Sciences and Engineering, University of Health and Rehabilitation Sciences Qingdao 266113 China.
Long-Long XiCollege of Chemistry and Chemical Engineering, Qingdao University Qingdao 266071 China xill@qdu.edu.cn.ORCID https://orcid.org/0009-0009-6433-6156
Ren-Rong LiuCollege of Pharmaceutical Sciences, Guizhou University Guiyang Guizhou 550025 China renrongliu@qdu.edu.cn.ORCID https://orcid.org/0000-0002-6474-3909

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tetraarylethenes are important π-conjugated molecules with versatile applications in OLEDs, fluorescent probes, and aggregation-induced emission (AIE) luminogens. Access to chiral TAEs is largely limited to strategies relying on preinstalled chiral elements or post-synthetic resolution, restricting structural diversity and functional exploration. Herein, we report a CPA-catalysed atroposelective transfer hydrogenation enabling the direct construction of axially chiral TAEs

Identifiers

PMID42317674
PMCPMC13273454

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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.