Evidence map›Paper›PMID 26419598›Full record

ReviewMolecular diversity2016

Molecular diversity of spirooxindoles. Synthesis and biological activity.

Tetyana L Pavlovska, Ruslan Gr Redkin, Victoria V Lipson, Dmytro V Atamanuk

Abstract readReview
PubMed Publisher
In one paragraph

Review in Molecular diversity, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing 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

39 citing papers in PubMed.

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  16. Tri(Beilstein journal of organic chemistry · 2022
    Article
  17. Article
  18. Article
  19. Preparation of GO/SiORSC advances · 2021
    Article
  20. 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

4 authors.

Tetyana L PavlovskaState Scientific Institution, "Institute for Single Crystals" of National Academy of Sciences of Ukraine, Lenina Pr., 60, Kharkov, 61002, Ukraine. tetjanka1@yandex.ru.
Ruslan Gr RedkinNational University of Pharmacy, Pushkinska Str., 53, Kharkov, 61002, Ukraine. ruslan.red.chem@gmail.com.
Victoria V LipsonState Scientific Institution, "Institute for Single Crystals" of National Academy of Sciences of Ukraine, Lenina Pr., 60, Kharkov, 61002, Ukraine. lipson@ukr.net.
Dmytro V AtamanukDmytro Atamanyuk Mutabilis, 102 Av. Gaston Roussel, Romainville, 93230, France. 4dmytro@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Spirooxindoles are important synthetic targets possessing extended biological activity and drug discovery applications. This review focuses on the various strategies for the enantioselective synthesis of spirocyclic oxindoles relying on reports over the past decade and from earlier work. The spirooxindoles in this review are separated into three structural classes, and then further categorized into the method type from which the spirocycle is generated.

Indexed as

Cycloaddition ReactionHeterocyclic CompoundsIndolesMolecular StructureSpiro CompoundsHeterocyclic CompoundsIndolesSpiro CompoundsCycloadditionsDiversity-oriented synthesisDOSHighly functionalised moleculesIsatinMulticomponent reactions (MCRs)OxindolesSpiroheterocyclic systems

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.