Evidence map›Paper›PMID 38699275›Full record

ArticleChemical science2024

Photochemical three-component assembly of tri-substituted oxazoles through a carbenic phosphorus-nitrile hybrid ylide formation/trapping cascade.

Xingchen Ye, Huaijin Pan, Yong Huang, Jiean Chen, Zhaofeng Wang

Abstract read
In one paragraph

Article in Chemical science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Harnessing PNature communications · 2026
    Article
  2. Synthetic Strategies to Access Fluorinated Azoles.European journal of organic chemistry · 2025
    Article
  3. Synthesis of Oxazoles Containing CFMolecules (Basel, Switzerland) · 2024
    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.

Xingchen YeState Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University Changsha Hunan 410082 P. R. China zfwangchem@hnu.edu.cn.
Huaijin PanState Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University Changsha Hunan 410082 P. R. China zfwangchem@hnu.edu.cn.
Yong HuangDepartment of Chemistry, The Hong Kong University of Science and Technology Clear Water Bay Kowloon Hong Kong SAR P. R. China yonghuang@ust.hk.ORCID https://orcid.org/0000-0001-8377-8923
Jiean ChenPingshan Translational Medicine Center, Shenzhen Bay Laboratory Shenzhen 518118 P. R. China chenja@szbl.ac.cn.ORCID https://orcid.org/0000-0003-0703-5831
Zhaofeng WangState Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University Changsha Hunan 410082 P. R. China zfwangchem@hnu.edu.cn.ORCID https://orcid.org/0000-0002-0547-8172

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Construction of complex molecular skeletons with ubiquitous chemical feedstocks in a single transformation is highly appealing in organic synthesis. We report a novel visible-light-induced three-component reaction for the construction of complex 2,4,5-trisubstituted oxazoles, which are valuable in medicinal chemistry, from simple and readily available iodonium-phosphonium hybrid ylides, carboxylic acids, and nitriles. This reaction features a carbenic phosphorus-nitrile hybrid ylide formation/trapping cascade, in which a photo-generated α-phosphonium carbene acts as a sequence trigger. This catalyst- and additive-free transformation exhibits high efficiency and broad substrate scope for synthesizing diverse oxazoles.

Identifiers

PMID38699275
PMCPMC11062088

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.