Evidence map›Paper›PMID 26351178›Full record

ArticleMolecular diversity2016

A novel four- and pseudo-five-component reaction: unexpected efficient one-pot synthesis of 4H-thiopyran derivatives.

Akbar Mobinikhaledi, Mohammad Ali Bodaghifard, Sajad Asadbegi

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular diversity, 2016. 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
1.4field-weighted citation impact, top 21% of its field
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, 13 citations in OpenAlex.

  1. Review
  2. Recent Developments on Five-Component Reactions.Molecules (Basel, Switzerland) · 2021
    Review
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

3 authors at 1 institution in 1 country.

Akbar MobinikhalediDepartment of Chemistry, Faculty of Science, Arak University, 38156-88349, Arak, Iran.
Mohammad Ali BodaghifardDepartment of Chemistry, Faculty of Science, Arak University, 38156-88349, Arak, Iran. mbodaghi2007@yahoo.com.
Sajad AsadbegiDepartment of Chemistry, Faculty of Science, Arak University, 38156-88349, Arak, Iran.
Arak University · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A facile and convenient novel method is reported for the synthesis of substituted 4H-thiopyrans by reacting aldehydes, malononitrile, carbon disulfide, and primary amines at room temperature in the presence of triethylamine as a catalyst. This reaction affords the desired products in high purity and has advantages of excellent yields, simple work-up procedure, and short reaction time.

Indexed as

AldehydesCarbon DisulfideCatalysisChemistry Techniques, SyntheticEthylaminesNitrilesPyransSulfhydryl CompoundsTemperatureAldehydesCarbon DisulfidedicyanmethaneEthylaminesNitrilesPyransSulfhydryl CompoundsthiopyrantriethylamineIsothiocyanateMCRMichael additionMulticomponent reactionOne-pot reactionThiopyrans

Identifiers

PMID26351178
OpenAlexW1425109641

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.