Evidence map›Paper›PMID 29728870›Full record

ReviewMolecular diversity2018

Nucleophilic ring opening reactions of aziridines.

Rabia Akhtar, Syed Ali Raza Naqvi, Ameer Fawad Zahoor, Sameera Saleem

Abstract readReview
PubMed Publisher
In one paragraph

Review in Molecular diversity, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. Article
  2. Article
  3. Fused-Linked and Spiro-Linked N-Containing Heterocycles.International journal of molecular sciences · 2025
    Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Toward asymmetric aziridination with an iron complex supported by aDalton transactions (Cambridge, England : 2003) · 2022
    Article
  12. Electrophilic Aminating Agents in Total Synthesis.Angewandte Chemie (International ed. in English) · 2021
    Review
  13. Article
  14. Article
  15. Synthetic Applications of Aziridinium Ions.Molecules (Basel, Switzerland) · 2021
    Review
  16. Alkylative Aziridine Ring-Opening Reactions.Molecules (Basel, Switzerland) · 2021
    Article
  17. Article
  18. Article
  19. Review
  20. 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.

Rabia AkhtarDepartment of Chemistry, Government College University Faisalabad, Faisalabad, 38000, Pakistan.
Syed Ali Raza NaqviDepartment of Chemistry, Government College University Faisalabad, Faisalabad, 38000, Pakistan.
Ameer Fawad ZahoorDepartment of Chemistry, Government College University Faisalabad, Faisalabad, 38000, Pakistan. fawad.zahoor@gcuf.edu.pk.
Sameera SaleemDepartment of Chemistry, Government College University Faisalabad, Faisalabad, 38000, Pakistan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aziridine ring opening reactions have gained tremendous importance in the synthesis of nitrogen containing biologically active molecules. During recent years, a great effort has been put forward by scientists toward unique bond construction methodologies via ring opening of aziridines. In this regard, a wide range of chiral metal- and organo-catalyzed desymmetrization reactions of aziridines have been reported with carbon, sulfur, oxygen, nitrogen, halogen, and other nucleophiles. In this review, an outline of methodologies adopted by a number of scientists during 2013-2017 for aziridine ring opening reactions as well as their synthetic applications is described.

Indexed as

AziridinesStereoisomerismAziridinesAziridineBiologically active compoundsEnantioselective synthesisMethodology developmentRing opening reactions

Identifiers

What OpenQuestion holds

Textmetadata
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.