Evidence map›Paper›PMID 41102917›Full record

ArticleChemistry, an Asian journal2025

Total Syntheses of Sappanin-Based Natural Products Enabled by Pattern Recognition Analysis and Brominative Aromatization.

Wei-Ting Zhao, Jing-Yu Liang, Yen-Ku Wu

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Chemistry, an Asian journal, 2025. 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.

  1. Article
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.

Wei-Ting ZhaoDepartment of Applied Chemistry and Center for Emergent Functional Matter Science, National Yang Ming Chiao Tung University, 1001 University Road, Hsinchu, 30010, Taiwan.
Jing-Yu LiangDepartment of Applied Chemistry and Center for Emergent Functional Matter Science, National Yang Ming Chiao Tung University, 1001 University Road, Hsinchu, 30010, Taiwan.
Yen-Ku WuDepartment of Applied Chemistry and Center for Emergent Functional Matter Science, National Yang Ming Chiao Tung University, 1001 University Road, Hsinchu, 30010, Taiwan.ORCID https://orcid.org/0000-0002-9269-7444

Funding

National Science and Technology Council NSTC 112-2628-M-A49-004-MY3National Science and Technology Council NSTC 114-2113-M-A49-010-MY3
6 · The paper itself

Abstract

Described is a concise route to caesappins A and B, urolithin C, and protosappanin A, which share a common sappanin core. An arylation of a cyclic vinylogous ester and a brominative aromatization were applied to construct a privileged intermediate, which was subsequently converted to the target natural products through strategic coupling reactions.

Indexed as

ArylationBrominative aromatizationPattern‐recognition analysisSappaninTotal synthesis

Identifiers

PMID41102917
PMCPMC12696778

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.