Evidence map›Paper›PMID 30836604›Full record

ArticleMolecules (Basel, Switzerland)2019

One-Pot NBS-Promoted Synthesis of Imidazoles and Thiazoles from Ethylarenes in Water.

Liang Chen, Huajian Zhu, Jiang Wang, Hong Liu

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. 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

4 authors.

Liang ChenSchool of Pharmacy, China Pharmaceutical University, Nanjing 210009, Jiangsu, China. zhulinfengcl@163.com.
Huajian ZhuSchool of Pharmacy, China Pharmaceutical University, Nanjing 210009, Jiangsu, China. cpuzhj@163.com.
Jiang WangState Key Laboratory of Drug Research and CAS Key Laboratory of Receptor Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, Shanghai, China. jwang@simm.ac.cn.
Hong LiuSchool of Pharmacy, China Pharmaceutical University, Nanjing 210009, Jiangsu, China. hliu@simm.ac.cn.

Funding

National Natural Science Foundation of China 81620108027, 21632008, and 21672231
6 · The paper itself

Abstract

A facile and eco-friendly method has been developed for the synthesis of imidazoles and thiazoles from ethylarenes in water. The reaction proceeds via in situ formation of α-bromoketone using NBS as a bromine source as well as an oxidant, followed by trapping with suitable nucleophiles to provide the corresponding products in good yields under metal-free conditions.

Indexed as

BromineBromosuccinimideImidazolesMolecular StructureSolventsTemperatureThiazolesTime FactorsWaterBromineBromosuccinimideImidazolesSolventsThiazolesWaterNBSnitrogen-containing heterocycleone-potwater

Identifiers

PMID30836604
PMCPMC6429224

What OpenQuestion holds

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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.