Evidence map›Paper›PMID 31491721›Full record

ArticleiScience2019

Synthesis of Biaryls via Decarbonylative Palladium-Catalyzed Suzuki-Miyaura Cross-Coupling of Carboxylic Acids.

Chengwei Liu, Chong-Lei Ji, Zhi-Xin Qin, Xin Hong, Michal Szostak

Open access · goldAbstract read
In one paragraph

Article in iScience, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
6.8field-weighted citation impact, top 2% 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

17 citing papers in PubMed, 92 citations in OpenAlex.

  1. Article
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  3. Aryl Acid-Alcohol Cross-Coupling: C(spJournal of the American Chemical Society · 2025
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  12. Decarbonylative Sulfide Synthesis from Carboxylic Acids and Thioesters via Cross-Over C-S Activation and Acyl Capture.Organic chemistry frontiers : an international journal of organic chemistry · 2021
    Article
  13. Article
  14. Article
  15. Article
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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 at 2 institutions in 2 countries.

Chengwei LiuDepartment of Chemistry, Rutgers University, 73 Warren Street, Newark, NJ 07102, USA.
Chong-Lei JiDepartment of Chemistry, Zhejiang University, Hangzhou 310027, China.
Zhi-Xin QinDepartment of Chemistry, Zhejiang University, Hangzhou 310027, China.
Xin HongDepartment of Chemistry, Zhejiang University, Hangzhou 310027, China. Electronic address: hxchem@zju.edu.cn.
Michal SzostakCollege of Chemistry and Chemical Engineering and Key Laboratory of Auxiliary Chemistry and Technology for Chemical Industry, Ministry of Education, Shaanxi University of Science and Technology, Xi'an 710021, China; Department of Chemistry, Rutgers University, 73 Warren Street, Newark, NJ 07102, USA. Electronic address: michal.szostak@rutgers.edu.
Zhejiang University · CNRutgers, The State University of New Jersey · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The biaryl motif is a building block in many drugs, agrochemicals, and materials, and as such it is highly desirable as a synthesis target. The state-of-the-art process for biaryl synthesis from ubiquitous carboxylic acids is decarboxylative cross-coupling involving loss of carbon dioxide (CO

Indexed as

CatalysisChemistryOrganic Chemistry

Identifiers

PMID31491721
PMCPMC6731188
OpenAlexW2969080910

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.