Evidence map›Paper›PMID 40317269›Full record

ArticleThe Journal of organic chemistry2025

Photocatalytic Nitrene Radical Anion Generation from Sulfonyl Azides for Intermolecular Aziridination of Unactivated Alkenes.

Dennis Dam, Joeri Schoenmakers, Elisabeth Bouwman, Jeroen D C Codée

Abstract read
In one paragraph

Article in The Journal of organic chemistry, 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. Article
  2. Synthesis and Application of Bioactive N-Functionalized Aziridines.Angewandte Chemie (International ed. in English) · 2025
    Review
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

4 authors.

Dennis DamLeiden Institute of Chemistry, Universiteit Leiden, 2333 CC Leiden, The Netherlands.ORCID 0000-0002-2510-9913
Joeri SchoenmakersLeiden Institute of Chemistry, Universiteit Leiden, 2333 CC Leiden, The Netherlands.
Elisabeth BouwmanLeiden Institute of Chemistry, Universiteit Leiden, 2333 CC Leiden, The Netherlands.
Jeroen D C CodéeLeiden Institute of Chemistry, Universiteit Leiden, 2333 CC Leiden, The Netherlands.ORCID 0000-0003-3531-2138

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aziridines are important structures in the contemporary organic synthesis and are used for several biological applications. Herein, we show that aziridines can be readily synthesized from alkenes by the reductive activation of sulfonyl azides, mediated by photoredox catalysis. Mechanistic studies indicate that the reaction proceeds through reactive nitrene radical anions instead of the more commonly encountered triplet nitrenes. A substrate scope is performed that showed good functional group compatibility.

Identifiers

PMID40317269
PMCPMC12090207

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.