Evidence map›Paper›PMID 36144635›Full record

ArticleMolecules (Basel, Switzerland)2022

Synthesis of Carbonyl-Containing Oxindoles via Ni-Catalyzed Reductive Aryl-Acylation and Aryl-Esterification of Alkenes.

Zhengtian Ding, Wangqing Kong

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2022. 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
1.0field-weighted citation impact, top 28% of its field
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, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

2 authors at 1 institution in 1 country.

Zhengtian DingThe Institute for Advanced Studies (IAS), Wuhan University, Wuhan 430072, China.
Wangqing KongThe Institute for Advanced Studies (IAS), Wuhan University, Wuhan 430072, China.ORCID 0000-0003-3260-0097
Wuhan University · CN

Funding

GuangDong Basic and Applied Basic Research Foundation 2022A1515010246National Natural Science Foundation of China 22171215
6 · The paper itself

Abstract

Carbonyl-containing oxindoles are ubiquitous core structures present in many biologically active natural products and pharmaceutical molecules. Nickel-catalyzed reductive aryl-acylation of alkenes using aryl anhydrides or alkanoyl chlorides as acyl sources is developed, providing 3,3-disubstituted oxindoles bearing ketone functionality at the 3-position. Moreover, nickel-catalyzed reductive aryl-esterification of alkenes using chloroformate as ester sources is further developed, affording 3,3-disubstituted oxindoles bearing ester functionality at the 3-position. This strategy has the advantages of good yields and high functional group compatibility.

Indexed as

AlkenesBiological ProductsAcylationAnhydridesCatalysisChloridesEsterificationEstersKetonesMolecular StructureNickelOxindolesPharmaceutical PreparationsAlkenesAnhydridesBiological ProductsChloridesEstersKetonesNickelOxindolesPharmaceutical Preparationsaryl-acylationaryl-esterificationnickel catalysisoxindolesreductive coupling reaction

Identifiers

PMID36144635
PMCPMC9503384
OpenAlexW4296016149

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.