Evidence map›Paper›PMID 28406463›Full record

ArticleMolecules (Basel, Switzerland)2017

Synthesis of Pyrrolo[1,2-a]pyrimidine Enantiomers via Domino Ring-Closure followed by Retro Diels-Alder Protocol.

Beáta Fekete, Márta Palkó, Matti Haukka, Ferenc Fülöp

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2017. 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. Synthesis of NovelMolecules (Basel, Switzerland) · 2019
    Article
  2. Special Issue: Asymmetric Synthesis 2017.Molecules (Basel, Switzerland) · 2017
    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.

Beáta FeketeInstitute of Pharmaceutical Chemistry, University of Szeged, Eötvös utca 6, Szeged H-6720, Hungary. fekete.beata@pharm.u-szeged.hu.
Márta PalkóInstitute of Pharmaceutical Chemistry, University of Szeged, Eötvös utca 6, Szeged H-6720, Hungary. palko@pharm.u-szeged.hu.
Matti HaukkaDepartment of Chemistry, University of Jyväskylä, FIN-40014 Turku, Finland. matti.o.haukka@jyu.fi.
Ferenc FülöpInstitute of Pharmaceutical Chemistry, University of Szeged, Eötvös utca 6, Szeged H-6720, Hungary. fulop@pharm.u-szeged.hu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

From 2-aminonorbornene hydroxamic acids, a simple and efficient method for the preparation of pyrrolo[1,2-

Indexed as

Chemistry Techniques, SyntheticCrystallography, X-RayHydroxamic AcidsMagnetic Resonance SpectroscopyModels, MolecularMolecular StructurePyrimidinesStereoisomerismHydroxamic AcidsPyrimidinesdomino reactionshydroxamic acidmicrowave chemistryN-heterocyclesretro Diels-Alder reaction

Identifiers

PMID28406463
PMCPMC6154686

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.