Evidence map›Paper›PMID 28675476›Full record

ArticleChemistry (Weinheim an der Bergstrasse, Germany)2017

Nitrene Radical Intermediates in Catalytic Synthesis.

Petrus F Kuijpers, Jarl Ivar van der Vlugt, Sven Schneider, Bas de Bruin

Abstract read
In one paragraph

Article in Chemistry (Weinheim an der Bergstrasse, Germany), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing 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

66 citing papers in PubMed.

  1. Photochemical Cascade Nitrile Activation via a Carbene-Nitrene Relay.Angewandte Chemie (International ed. in English) · 2026
    Article
  2. Article
  3. Photoactive Iminobismuthanes for Catalytic C-H Amination.Journal of the American Chemical Society · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Photogeneration and Visualization of a Surface-Stabilized Dinitrene.Angewandte Chemie (International ed. in English) · 2025
    Article
  11. Article
  12. P-P CouplingJournal of the American Chemical Society · 2025
    Article
  13. Article
  14. Article
  15. HowJACS Au · 2023
    Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article

6 more citing papers are in PubMed but not listed here.

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.

Petrus F KuijpersVan 't Hoff Institute for Molecular Sciences (HIMS), University of Amsterdam (UvA), Science Park 904, 1098 XH, Amsterdam, The Netherlands.
Jarl Ivar van der VlugtVan 't Hoff Institute for Molecular Sciences (HIMS), University of Amsterdam (UvA), Science Park 904, 1098 XH, Amsterdam, The Netherlands.ORCID http://orcid.org/0000-0003-0665-9239
Sven SchneiderInstitut für Anorganische Chemie, Universität Göttingen, Tammannstr. 4, 37077, Göttingen, Germany.
Bas de BruinVan 't Hoff Institute for Molecular Sciences (HIMS), University of Amsterdam (UvA), Science Park 904, 1098 XH, Amsterdam, The Netherlands.ORCID http://orcid.org/0000-0002-3482-7669

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nitrene radical complexes are reactive intermediates with discrete spin density at the nitrogen-atom of the nitrene moiety. These species have become important intermediates for organic synthesis, being invoked in a broad range of C-H functionalization and aziridination reactions. Nitrene radical complexes have intriguing electronic structures, and are best described as one-electron reduced Fischer type nitrenes. They can be generated by intramolecular single electron transfer to the "redox non-innocent" nitrene moiety at the metal. Nitrene radicals generated at open-shell cobalt(II) have thus far received most attention in terms of spectroscopic characterization, reactivity screening, catalytic nitrene-transfer reactions and (computational and experimental) mechanistic studies, but some interesting iron and precious metal catalysts have also been employed in related reactions involving nitrene radicals. In some cases, redox-active ligands are used to facilitate intramolecular single electron transfer from the complex to the nitrene moiety. Organic azides are among the most attractive nitrene precursors in this field, typically requiring pre-activated organic azides (e.g. RSO

Indexed as

C−H aminationelectronic structure-reactivity correlationsmetalloradical catalysisnoninnocent ligandsradicals

Identifiers

PMID28675476
PMCPMC5656926

What OpenQuestion holds

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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.