Evidence map›Paper›PMID 35310496›Full record

ArticleChemical science2022

Paired electrolysis enabled annulation for the quinolyl-modification of bioactive molecules.

Shiqi You, Mengyao Ruan, Cuifen Lu, Li Liu, Yue Weng, Guichun Yang, Shengchun Wang, Hesham Alhumade, Aiwen Lei, Meng Gao

Abstract read
In one paragraph

Article in Chemical science, 2022. 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. Article
  2. 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

10 authors.

Shiqi YouCollege of Chemistry and Chemical Engineering, Ministry of Education Key Laboratory for the Synthesis and Application of Organic Functional Molecules, Hubei University Wuhan 430062 P. R. China drmenggao@163.com.ORCID https://orcid.org/0000-0002-9785-6600
Mengyao RuanCollege of Chemistry and Chemical Engineering, Ministry of Education Key Laboratory for the Synthesis and Application of Organic Functional Molecules, Hubei University Wuhan 430062 P. R. China drmenggao@163.com.
Cuifen LuCollege of Chemistry and Chemical Engineering, Ministry of Education Key Laboratory for the Synthesis and Application of Organic Functional Molecules, Hubei University Wuhan 430062 P. R. China drmenggao@163.com.ORCID https://orcid.org/0000-0002-9040-7861
Li LiuCollege of Chemistry and Chemical Engineering, Ministry of Education Key Laboratory for the Synthesis and Application of Organic Functional Molecules, Hubei University Wuhan 430062 P. R. China drmenggao@163.com.ORCID https://orcid.org/0000-0002-3684-4032
Yue WengCollege of Chemistry and Chemical Engineering, Ministry of Education Key Laboratory for the Synthesis and Application of Organic Functional Molecules, Hubei University Wuhan 430062 P. R. China drmenggao@163.com.
Guichun YangCollege of Chemistry and Chemical Engineering, Ministry of Education Key Laboratory for the Synthesis and Application of Organic Functional Molecules, Hubei University Wuhan 430062 P. R. China drmenggao@163.com.
Shengchun WangCollege of Chemistry and Molecular Sciences and the Institute for Advanced Studies (IAS), Wuhan University Wuhan 430072 Hubei P. R. China aiwenlei@whu.edu.cn.
Hesham AlhumadeDepartment of Chemical and Materials Engineering, Faculty of Engineering, Center of Research Excellence in Renewable Energy and Power Systems, King Abdulaziz University Jeddah 21589 Saudi Arabia.
Aiwen LeiCollege of Chemistry and Molecular Sciences and the Institute for Advanced Studies (IAS), Wuhan University Wuhan 430072 Hubei P. R. China aiwenlei@whu.edu.cn.ORCID https://orcid.org/0000-0001-8417-3061
Meng GaoCollege of Chemistry and Chemical Engineering, Ministry of Education Key Laboratory for the Synthesis and Application of Organic Functional Molecules, Hubei University Wuhan 430062 P. R. China drmenggao@163.com.ORCID https://orcid.org/0000-0002-2662-3981

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A paired electrolysis enabled cascade annulation that enables the efficient synthesis of highly functionalized quinoline-substituted bioactive molecules from readily available starting materials is reported. Using this methodology, two goals, namely, the direct synthesis of quinolines and the introduction of quinoline moieties to bioactive molecules, can be simultaneously achieved in one simple operation. The use of electroreduction for the activation of isatin, together with the further anodic oxidation of KI to catalytically result in a cascade annulation, highlight the unique possibilities associated with electrochemical activation methods. This transformation can tolerate a wide range of functional groups and can also be used as a functionalization tactic in pharmaceutical research as well as other areas.

Identifiers

PMID35310496
PMCPMC8864700

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.