Evidence map›Paper›PMID 34576025›Full record

ReviewInternational journal of molecular sciences2021

3-Arylaziridine-2-carboxylic Acid Derivatives and (3-Arylaziridin-2-yl)ketones: The Aziridination Approaches.

Boriss Strumfs, Romans Uljanovs, Kirils Velikijs, Peteris Trapencieris, Ilze Strumfa

Abstract readReview
PubMed Full text at PMC Publisher
In one paragraph

Review in International journal of molecular sciences, 2021. 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. Review
  2. An Easy Route to Aziridine Ketones and Carbinols.International journal of molecular sciences · 2021
    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

5 authors.

Boriss StrumfsLatvian Institute of Organic Synthesis, 21 Aizkraukles Street, LV-1006 Riga, Latvia.
Romans UljanovsDepartment of Pathology, Riga Stradins University, 16 Dzirciema Street, LV-1007 Riga, Latvia.
Kirils VelikijsDepartment of Pathology, Riga Stradins University, 16 Dzirciema Street, LV-1007 Riga, Latvia.
Peteris TrapencierisLatvian Institute of Organic Synthesis, 21 Aizkraukles Street, LV-1006 Riga, Latvia.
Ilze StrumfaDepartment of Pathology, Riga Stradins University, 16 Dzirciema Street, LV-1007 Riga, Latvia.ORCID 0000-0002-7393-9524

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aziridination reactions represent a powerful tool in aziridine synthesis. Significant progress has been achieved in this field in the last decades, whereas highly functionalized aziridines including 3-arylated aziridine-2-carbonyl compounds play an important role in both medical and synthetic chemistry. For the reasons listed, in the current review we have focused on the ways to obtain 3-arylated aziridines and on the recent advances (mainly since the year 2000) in the methodology of the synthesis of these compounds via aziridination.

Indexed as

AziridinesCarboxylic AcidsIminesKetonesMolecular StructureStereoisomerismaziridineaziridine-2-carboxylic acidAziridinesCarboxylic AcidsIminesKetonesaziridinationaziridinescarbenesiminesnitrenes

Identifiers

PMID34576025
PMCPMC8469611

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.