Evidence map›Paper›PMID 42402184›Full record

ArticleAngewandte Chemie (International ed. in English)2026

A General and Scalable Chiral Surrogate Rotaxane Strategy for Highly Enantioenriched Mechanically Planar Chiral Rotaxanes.

Shang-Rui Lee, Yi-Hung Liu, Sheng-Hsien Chiu

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 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

3 authors.

Shang-Rui LeeDepartment of Chemistry, National Taiwan University, Taipei, Taiwan.
Yi-Hung LiuDepartment of Chemistry, National Taiwan University, Taipei, Taiwan.
Sheng-Hsien ChiuDepartment of Chemistry, National Taiwan University, Taipei, Taiwan.ORCID https://orcid.org/0000-0002-0040-1555

Funding

the National Science and Technology Council NSTC-114-2123-M-002-001
6 · The paper itself

Abstract

We report a general and modular chiral surrogate rotaxane (CSR) strategy for the synthesis of mechanically planar chiral rotaxanes (MPCRs) of high optical purity (ca. 99.6% ee). A diastereomeric CSR, readily separable by column chromatography, is first generated through an S

Indexed as

absolute configurationenantiopuremechanical chiralityrotaxanesurrogate

Identifiers

PMID42402184
PMCPMC13548897

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.