Evidence map›Paper›PMID 36349099›Full record

ArticleChemical science2022

Iminologous epoxide ring-closure.

Chieh-Hung Tien, Alan J Lough, Andrei K Yudin

Open access · diamondAbstract read
In one paragraph

Article in Chemical science, 2022. 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
0.5field-weighted citation impact, top 40% of its field
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, 5 citations in OpenAlex.

  1. Rapid Access to Conjugated Z,Z,Z-Trienes.Angewandte Chemie (International ed. in English) · 2025
    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

3 authors at 1 institution in 1 country.

Chieh-Hung TienDavenport Research Laboratories, Department of Chemistry, University of Toronto Toronto ON M5S 3H6 Canada andrei.yudin@utoronto.ca.ORCID https://orcid.org/0000-0002-7859-5804
Alan J LoughX-Ray Crystallography Laboratory, Department of Chemistry, University of Toronto Toronto ON M5S 3H6 Canada.
Andrei K YudinDavenport Research Laboratories, Department of Chemistry, University of Toronto Toronto ON M5S 3H6 Canada andrei.yudin@utoronto.ca.ORCID https://orcid.org/0000-0003-3170-9103
University of Toronto · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The discovery of new reactions enables chemists to attain a better understanding of fundamental chemical reactivity and push the boundaries of organic synthesis. Our understanding and manipulation of high-energy states such as reactive conformations, intermediates, and transition structures contribute to this field. Herein we interrogate epoxide ring-closure by inserting the C[double bond, length as m-dash]N functionality into a well-known precursor to nucleophilic epoxide ring-closure. The synthesis of tetrasubstituted, nitrile-tethered epoxides takes place

Identifiers

PMID36349099
PMCPMC9600474
OpenAlexW4308685395

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.