Evidence map›Paper›PMID 30471013›Full record

ArticleMolecular diversity2019

Synthesis of (E)-2-amino-N'-benzylidenehexahydroquinoline-3-carbohydrazide.

Milad Masoumi, Fahimeh Sadat Hosseini, Mohammad Bayat

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular diversity, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Milad MasoumiDepartment of Chemistry, Faculty of Science, Imam Khomeini International University, Qazvin, Iran.
Fahimeh Sadat HosseiniDepartment of Chemistry, Faculty of Science, Imam Khomeini International University, Qazvin, Iran.
Mohammad BayatDepartment of Chemistry, Faculty of Science, Imam Khomeini International University, Qazvin, Iran. bayat_mo@yahoo.com.ORCID http://orcid.org/0000-0002-5235-1203

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A one-pot, multi-component protocol for the synthesis of a new class of functionalized quinoline carbohydrazide derivatives via reaction of various anilines, dimedone, aromatic aldehydes, and cyanoacetohydrazide is described. The reactions are completed in the presence of catalytic amount of piperidine, respectively, in melt conditions and then in ethanol/water (1:1) as green solvent at 80 °C. Mild conditions, green medium, short reaction times, simple workup and purification process with no chromatographic technique, and good yields are the main advantages of this method.

Indexed as

CatalysisChemistry Techniques, SyntheticGreen Chemistry TechnologyHydrazinescarbohydrazideHydrazinesAnilinesAromatic aldehydesCyanoacetohydrazideDimedoneMulti-component protocolQuinoline carbohydrazide derivatives

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.