Evidence map›Paper›PMID 41311885›Full record

ArticleChemical science2026

Inherently chiral homo-heteracalixarenes: design and synthesis

Y-F Jiang, Y Zhang, S Tong, J Zhu, M-X Wang

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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.

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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

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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

5 authors.

Y-F JiangKey Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology (Ministry of Education), Department of Chemistry, Tsinghua University Beijing 100084 China tongshuo@mail.tsinghua.edu.cn http://mascl.group.
Y ZhangKey Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology (Ministry of Education), Department of Chemistry, Tsinghua University Beijing 100084 China tongshuo@mail.tsinghua.edu.cn http://mascl.group.
S TongKey Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology (Ministry of Education), Department of Chemistry, Tsinghua University Beijing 100084 China tongshuo@mail.tsinghua.edu.cn http://mascl.group.ORCID https://orcid.org/0000-0002-7982-2546
J ZhuLaboratory of Synthesis and Natural Products (LSPN), Institute of Chemical Sciences and Engineering, Ecole Polytechnique Fédéral de Lausanne, EPFL-SB-ISIC-LSPN BCH5304 CH-1015 Lausanne Switzerland.ORCID https://orcid.org/0000-0002-8390-6689
M-X WangKey Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology (Ministry of Education), Department of Chemistry, Tsinghua University Beijing 100084 China tongshuo@mail.tsinghua.edu.cn http://mascl.group.ORCID https://orcid.org/0000-0001-7112-0657

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent research has seen growing interest in synthesizing inherently chiral macrocycles, driven by their potential applications in chiral supramolecular chemistry. We present herein our design and synthesis of a series of novel inherently chiral macrocycles. These compounds, termed homo-heteracalixarenes, feature a 1,2-diphenylethyne fragment that replaces one of the aryl-heteroatom-aryl linkages found in classic heteracalix[4]aromatics.

Identifiers

PMID41311885
PMCPMC12650766

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