Evidence map›Paper›PMID 40880780›Full record

ArticleChemical science2025

Unveiling the migration reactivity of bicyclic diaziridines: enantioselective synthesis of chiral pyrazolines.

Zhili Liu, Lichao Ning, Bingqian Yang, Kaixuan Wang, Lili Lin, Xiaoming Feng

Abstract read
In one paragraph

Article in Chemical science, 2025. 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

6 authors.

Zhili LiuKey Laboratory of Green Chemistry & Technology, Ministry of Education, College of Chemistry, Sichuan University Chengdu 610064 P. R. China lililin@scu.edu.cn xmfeng@scu.edu.cn.
Lichao NingKey Laboratory of Green Chemistry & Technology, Ministry of Education, College of Chemistry, Sichuan University Chengdu 610064 P. R. China lililin@scu.edu.cn xmfeng@scu.edu.cn.
Bingqian YangKey Laboratory of Green Chemistry & Technology, Ministry of Education, College of Chemistry, Sichuan University Chengdu 610064 P. R. China lililin@scu.edu.cn xmfeng@scu.edu.cn.
Kaixuan WangKey Laboratory of Green Chemistry & Technology, Ministry of Education, College of Chemistry, Sichuan University Chengdu 610064 P. R. China lililin@scu.edu.cn xmfeng@scu.edu.cn.
Lili LinKey Laboratory of Green Chemistry & Technology, Ministry of Education, College of Chemistry, Sichuan University Chengdu 610064 P. R. China lililin@scu.edu.cn xmfeng@scu.edu.cn.ORCID https://orcid.org/0000-0001-8723-6793
Xiaoming FengKey Laboratory of Green Chemistry & Technology, Ministry of Education, College of Chemistry, Sichuan University Chengdu 610064 P. R. China lililin@scu.edu.cn xmfeng@scu.edu.cn.ORCID https://orcid.org/0000-0003-4507-0478

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ring-opening/cyclization represents a classic reaction of bicyclic diaziridines. In this study, an unprecedented ring-opening/migration cascade process was discovered in the reaction between bicyclic diaziridines and donor-acceptor (D-A) cyclopropanes. By employing a chiral

Identifiers

PMID40880780
PMCPMC12372524

What OpenQuestion holds

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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.