Evidence map›Paper›PMID 36234770›Full record

ArticleMolecules (Basel, Switzerland)2022

Homocouplings of Sodium Arenesulfinates: Selective Access to Symmetric Diaryl Sulfides and Diaryl Disulfides.

Xin-Zhang Yu, Wen-Long Wei, Yu-Lan Niu, Xing Li, Ming Wang, Wen-Chao Gao

Open access · goldAbstract read
PubMed Full text at PMC Publisher
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
1.1field-weighted citation impact, top 26% 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, 10 citations in OpenAlex.

  1. Review
  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

6 authors at 3 institutions in 1 country.

Xin-Zhang YuDepartment of Chemistry and Chemical Engineering, Taiyuan Institute of Technology, Taiyuan 030008, China.
Wen-Long WeiDepartment of Biomedical Engineering, Taiyuan University of Technology, Taiyuan 030024, China.
Yu-Lan NiuDepartment of Chemistry and Chemical Engineering, Taiyuan Institute of Technology, Taiyuan 030008, China.
Xing LiDepartment of Biomedical Engineering, Taiyuan University of Technology, Taiyuan 030024, China.
Ming WangSchool of Chemistry and Molecular Engineering, East China Normal University, 3663, Shanghai 200062, China.
Wen-Chao GaoDepartment of Biomedical Engineering, Taiyuan University of Technology, Taiyuan 030024, China.ORCID 0000-0002-1382-6210
East China Normal University · CNTaiyuan Institute of Technology · CNTaiyuan University of Technology · CN

Funding

National Natural Science Foundation of China 21901179
6 · The paper itself

Abstract

Symmetrical diaryl sulfides and diaryl disulfides have been efficiently and selectively constructed via the homocoupling of sodium arenesulfinates. The selectivity of products relied on the different reaction systems: symmetrical diaryl sulfides were predominately obtained under the Pd(OAc)

Indexed as

DisulfidesSulfidesCatalysisMolecular StructureSodiumDisulfidesSodiumSulfidesdiaryl disulfidesdiaryl sulfideshomocouplingsodium arenesulfinatessymmetric

Identifiers

PMID36234770
PMCPMC9571168
OpenAlexW4296641849

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.