Evidence map›Paper›PMID 39886069›Full record

ReviewRSC advances2025

Asymmetric photoreactions catalyzed by chiral ketones.

Bao-Ji Bian, Liu Yang, Li-Xin Qiao, Qiang Zhang, Wei He

Abstract readReview
In one paragraph

Review in RSC advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. N-Aryl Acridone Derivatives as Effective Catalysts for Energy Transfer Reactions.Chemistry (Weinheim an der Bergstrasse, Germany) · 2026
    Article
  2. 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

5 authors.

Bao-Ji BianShaanxi Province Key Laboratory of Catalytic, School of Chemical and Environmental Science, Shaanxi University of Technology Hanzhong 723001 P. R. China zhangqiang22@126.com.
Liu YangDepartment of Chemistry, School of Pharmacy, Air Force Medical University Xi'an 710032 P. R. China weihechem@fmmu.edu.cn.
Li-Xin QiaoDepartment of Chemistry, School of Pharmacy, Air Force Medical University Xi'an 710032 P. R. China weihechem@fmmu.edu.cn.
Qiang ZhangShaanxi Province Key Laboratory of Catalytic, School of Chemical and Environmental Science, Shaanxi University of Technology Hanzhong 723001 P. R. China zhangqiang22@126.com.ORCID https://orcid.org/0000-0001-6107-6584
Wei HeShaanxi Province Key Laboratory of Catalytic, School of Chemical and Environmental Science, Shaanxi University of Technology Hanzhong 723001 P. R. China zhangqiang22@126.com.ORCID https://orcid.org/0000-0002-6703-6855

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Asymmetric catalytic reactions are essential for synthesizing chiral drugs and fine chemicals, with their stereoselectivity influenced significantly by interactions between catalysts and substrates. Ketone catalysts have garnered considerable attention in the realm of asymmetric photoreactions because of their highly controllable structures, ease of availability, and environmental friendliness. This review highlights the application of various reported ketone catalysts in a range of asymmetric photoreactions, including [2 + 2] photocycloaddition, photoderacemization, photochemical rearrangement, asymmetric electrophilic amination, and asymmetric alkylation of aldehydes. This review discusses the design concepts, catalytic mechanisms, as well as the advantages and limitations of these catalysts within each reaction. The aim is to provide valuable insights for developing more effective asymmetric catalytic systems.

Identifiers

PMID39886069
PMCPMC11781534

What OpenQuestion holds

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LicenceCC BY-NC
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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.