Evidence map›Paper›PMID 42006478›Full record

ArticleChemical science2026

Photoinduced deacylative epoxidation of ketone derivatives with allylic peroxides.

Jiangtao Lin, Mingqian Zhou, Ziyang Li, Jiang Duan, Xiaoyu Liu, Yue Wang, Chao Shu

Abstract read
PubMed Full text at PMC Publisher
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
–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

7 authors.

Jiangtao LinState Key Laboratory of Green Pesticide, Engineering Research Center of Photoenergy Utilization for Pollution Control and Carbon Reduction, CCNU-uOttawa Joint Research Centre, College of Chemistry, Central China Normal University 152 Luoyu Road Wuhan Hubei 430079 China chaoshu@ccnu.edu.cn.
Mingqian ZhouState Key Laboratory of Green Pesticide, Engineering Research Center of Photoenergy Utilization for Pollution Control and Carbon Reduction, CCNU-uOttawa Joint Research Centre, College of Chemistry, Central China Normal University 152 Luoyu Road Wuhan Hubei 430079 China chaoshu@ccnu.edu.cn.
Ziyang LiState Key Laboratory of Green Pesticide, Engineering Research Center of Photoenergy Utilization for Pollution Control and Carbon Reduction, CCNU-uOttawa Joint Research Centre, College of Chemistry, Central China Normal University 152 Luoyu Road Wuhan Hubei 430079 China chaoshu@ccnu.edu.cn.
Jiang DuanState Key Laboratory of Green Pesticide, Engineering Research Center of Photoenergy Utilization for Pollution Control and Carbon Reduction, CCNU-uOttawa Joint Research Centre, College of Chemistry, Central China Normal University 152 Luoyu Road Wuhan Hubei 430079 China chaoshu@ccnu.edu.cn.
Xiaoyu LiuState Key Laboratory of Green Pesticide, Engineering Research Center of Photoenergy Utilization for Pollution Control and Carbon Reduction, CCNU-uOttawa Joint Research Centre, College of Chemistry, Central China Normal University 152 Luoyu Road Wuhan Hubei 430079 China chaoshu@ccnu.edu.cn.
Yue WangState Key Laboratory of Green Pesticide, Engineering Research Center of Photoenergy Utilization for Pollution Control and Carbon Reduction, CCNU-uOttawa Joint Research Centre, College of Chemistry, Central China Normal University 152 Luoyu Road Wuhan Hubei 430079 China chaoshu@ccnu.edu.cn.
Chao ShuState Key Laboratory of Green Pesticide, Engineering Research Center of Photoenergy Utilization for Pollution Control and Carbon Reduction, CCNU-uOttawa Joint Research Centre, College of Chemistry, Central China Normal University 152 Luoyu Road Wuhan Hubei 430079 China chaoshu@ccnu.edu.cn.ORCID https://orcid.org/0000-0002-4722-2714

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epoxide compounds represent a privileged scaffold with diverse applications in organic synthesis, pharmaceuticals, agrochemicals, and materials science. However, the available routes to obtain such high-value structures from feedstocks, such as ketones, remain less developed. In this work, we report an alternative deacylative epoxidation of ketones using allylic peroxides to produce fused epoxides

Identifiers

PMID42006478
PMCPMC13089765

What OpenQuestion holds

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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.