Evidence map›Paper›PMID 34805095›Full record

ArticleFrontiers in chemistry2021

Highly Diastereoselective Synthesis of Tetrahydroquinoline Derivatives

Taiwei Dong, Peifeng Wei, Min Li, Feng Gao, Yuan Qin

Abstract read
In one paragraph

Article in Frontiers in chemistry, 2021. 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, crystal structure and Hirshfeld surface analysis of ethyl (Acta crystallographica. Section E, Crystallographic communications · 2025
    Article
  2. 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

5 authors.

Taiwei DongCollege of Pharmacy, Shaanxi University of Chinese Medicine, Xianyang, China.
Peifeng WeiCollege of Pharmacy, Shaanxi University of Chinese Medicine, Xianyang, China.
Min LiCollege of Pharmacy, Shaanxi University of Chinese Medicine, Xianyang, China.
Feng GaoCollege of Pharmacy, Shaanxi University of Chinese Medicine, Xianyang, China.
Yuan QinState Key Laboratory of Military Stomatology and National Clinical Research Center for Oral Diseases and Shaanxi Clinical Research Center for Oral Diseases, Department of Orthodontics, School of Stomatology, The Fourth Military Medical University, Xi'an, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As a privileged structural motif, tetrahydroquinoline skeletons widely exist in biologically active natural products and pharmaceuticals. In this protocol, a highly diastereoselective [4 + 2] annulation of

Indexed as

16-conjugate additionAza-Michaelmulti-substituted alkenesp-quinone methidestetrahydroquinolines

Identifiers

PMID34805095
PMCPMC8595915

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.