Evidence map›Paper›PMID 30795610›Full record

ArticleMolecules (Basel, Switzerland)2019

Synthesis of Novel

Márta Palkó, Mohamed El Haimer, Zsanett Kormányos, Ferenc Fülöp

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Triazole analogues as potential pharmacological agents: a brief review.Future journal of pharmaceutical sciences · 2021
    Review
  6. 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.

Márta PalkóInstitute of Pharmaceutical Chemistry, University of Szeged, Interdisciplinary excellence centre, Eötvös utca 6, Szeged H-6720, Hungary. palko@pharm.u-szeged.hu.
Mohamed El HaimerInstitute of Pharmaceutical Chemistry, University of Szeged, Interdisciplinary excellence centre, Eötvös utca 6, Szeged H-6720, Hungary. el.haimer.mohamed@pharm.u-szeged.hu.
Zsanett KormányosInstitute of Pharmaceutical Chemistry, University of Szeged, Interdisciplinary excellence centre, Eötvös utca 6, Szeged H-6720, Hungary. zsani0424@gmail.com.
Ferenc FülöpInstitute of Pharmaceutical Chemistry, University of Szeged, Interdisciplinary excellence centre, Eötvös utca 6, Szeged H-6720, Hungary. fulop@pharm.u-szeged.hu.ORCID 0000-0003-1066-5287

Funding

Országos Tudományos Kutatási Alapprogramok K 115731
6 · The paper itself

Abstract

An uncomplicated, high-yielding synthetic route has been developed to constitute complicated heterocycles, applying domino, click and retro-Diels⁻Alder (RDA) reaction sequences. Starting from 2-aminocarboxamides, a new set of isoindolo[2,1-

Indexed as

Chemistry Techniques, SyntheticClick ChemistryCyclizationCycloaddition ReactionHumansMagnetic Resonance SpectroscopyMolecular StructureNorbornanesQuinazolinonesTriazolesNorbornanesQuinazolinonesTriazolesclick reactiondomino ring closureRDA reactionregioselectivitystereoselectivitytraceless chirality transfer

Identifiers

PMID30795610
PMCPMC6412576

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.