Evidence map›Paper›PMID 35516904›Full record

ArticleRSC advances2019

Synthesis and anticancer activity novel dimeric azatriperoxides.

Nataliya N Makhmudiyarova, Irina R Ishmukhametova, Lilya U Dzhemileva, Tatyana V Tyumkina, Vladimir A D'yakonov, Askhat G Ibragimov, Usein M Dzhemilev

Abstract read
In one paragraph

Article in RSC advances, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Synthesis of cyclic aza-peroxides (microreview).Chemistry of heterocyclic compounds · 2021
    Article
  4. Article
  5. 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

7 authors.

Nataliya N MakhmudiyarovaInstitute of Petrochemistry and Catalysis, Russian Academy of Sciences 141 Prospekt Oktyabrya 450075 Ufa Russian Federation natali-mnn@mail.ru dzhemilev@mail.ru.ORCID https://orcid.org/0000-0003-1952-4173
Irina R IshmukhametovaInstitute of Petrochemistry and Catalysis, Russian Academy of Sciences 141 Prospekt Oktyabrya 450075 Ufa Russian Federation natali-mnn@mail.ru dzhemilev@mail.ru.
Lilya U DzhemilevaInstitute of Petrochemistry and Catalysis, Russian Academy of Sciences 141 Prospekt Oktyabrya 450075 Ufa Russian Federation natali-mnn@mail.ru dzhemilev@mail.ru.
Tatyana V TyumkinaInstitute of Petrochemistry and Catalysis, Russian Academy of Sciences 141 Prospekt Oktyabrya 450075 Ufa Russian Federation natali-mnn@mail.ru dzhemilev@mail.ru.
Vladimir A D'yakonovInstitute of Petrochemistry and Catalysis, Russian Academy of Sciences 141 Prospekt Oktyabrya 450075 Ufa Russian Federation natali-mnn@mail.ru dzhemilev@mail.ru.
Askhat G IbragimovInstitute of Petrochemistry and Catalysis, Russian Academy of Sciences 141 Prospekt Oktyabrya 450075 Ufa Russian Federation natali-mnn@mail.ru dzhemilev@mail.ru.
Usein M DzhemilevInstitute of Petrochemistry and Catalysis, Russian Academy of Sciences 141 Prospekt Oktyabrya 450075 Ufa Russian Federation natali-mnn@mail.ru dzhemilev@mail.ru.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An efficient method was developed for the synthesis of tetra(spirocycloalkane)-substituted α,ω-di(1,2,4,5,7,8-hexaoxa-10-azacycloundecan-10-yl)alkanes by a ring transformation reaction of 3,6-di(spirocycloalkane)-substituted 1,2,4,5,7,8,10-heptaoxacycloundecanes with α,ω-alkanediamines (1,4-butane-, 1,5-pentane-, 1,7-heptane-, 1,8-octane- and 1,10-decanediamines) catalyzed by Sm(NO

Identifiers

PMID35516904
PMCPMC9064891

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.