Evidence map›Paper›PMID 34040730›Full record

ArticleChemical science2021

Radical-based functionalization-oriented construction: rapid assembly of azaarene-substituted highly functionalized pyrroles.

Weigao Hu, Qiangqiang Zhan, Hongwei Zhou, Shanshan Cao, Zhiyong Jiang

Abstract read
In one paragraph

Article in Chemical science, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Dicyanopyrazine: 10th Anniversary in Photoredox Catalysis.Chemical record (New York, N.Y.) · 2025
    Article
  2. Article
  3. 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

5 authors.

Weigao HuInternational Scientific and Technological Cooperation Base of Chiral Chemistry, Henan University Kaifeng Henan 475004 P. R. China jiangzhiyong@htu.edu.cn.
Qiangqiang ZhanInternational Scientific and Technological Cooperation Base of Chiral Chemistry, Henan University Kaifeng Henan 475004 P. R. China jiangzhiyong@htu.edu.cn.
Hongwei ZhouCollege of Biological, Chemical Sciences and Engineering, Jiaxing University Jiaxing Zhejiang P. R. China 314001.ORCID https://orcid.org/0000-0001-8308-960X
Shanshan CaoSchool of Chemistry and Chemical Engineering, Henan Normal University Xinxiang Henan 453007 P. R. China caoshanshan@htu.edu.cn.
Zhiyong JiangInternational Scientific and Technological Cooperation Base of Chiral Chemistry, Henan University Kaifeng Henan 475004 P. R. China jiangzhiyong@htu.edu.cn.ORCID https://orcid.org/0000-0002-6350-7429

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Totally different functionalization and construction as two fundamental synthetic protocols have long been applied to furnish azaarene variants. Here, a novel radical-based functionalization-oriented construction strategy by exploiting the electronic properties of azaarenes and the high reactivity of radicals is developed. Under a photoredox catalysis platform, the robust ability of such an artful combination of functionalization with construction is disclosed in the synthesis of valuable 3-azaarene-substituted densely functionalized pyrroles. In addition to the ability to use the readily accessible feedstocks, the high synthetic efficiency and the good functional group tolerance, the substrate scope is broad (81 examples) resulting from the capability to flexibly replace the types of azaarenes and other substituents. Control experiments and density functional theory (DFT) calculations elucidate the plausible mechanism involving the reaction pathways and the important role of NaH

Identifiers

PMID34040730
PMCPMC8132952

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.