Evidence map›Paper›PMID 36756330›Full record

ArticleChemical science2023

A Ni-catalyzed asymmetric C(sp)-P cross-coupling reaction for the synthesis of P-stereogenic alkynylphosphines.

Bin Zhang, Wen-Qing Zhou, Xu-Teng Liu, Yingying Sun, Qing-Wei Zhang

Open access · diamondAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Chemical science, 2023. 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
2.9field-weighted citation impact, top 9% 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

2 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. 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

5 authors at 1 institution in 1 country.

Bin ZhangDepartment of Chemistry, University of Science and Technology of China Hefei 230026 China qingweiz@ustc.edu.cn.
Wen-Qing ZhouDepartment of Chemistry, University of Science and Technology of China Hefei 230026 China qingweiz@ustc.edu.cn.
Xu-Teng LiuDepartment of Chemistry, University of Science and Technology of China Hefei 230026 China qingweiz@ustc.edu.cn.
Yingying SunDepartment of Chemistry, University of Science and Technology of China Hefei 230026 China qingweiz@ustc.edu.cn.
Qing-Wei ZhangDepartment of Chemistry, University of Science and Technology of China Hefei 230026 China qingweiz@ustc.edu.cn.ORCID https://orcid.org/0000-0002-8577-6304
University of Science and Technology of China · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Due to the high reactivity of the triple bond, P-stereogenic alkynylphosphines could be easily derivatized, serving as universal building blocks for structurally diverse phosphine compounds. However, the synthesis of alkynylphosphines

Identifiers

PMID36756330
PMCPMC9891383
OpenAlexW4313623154

What OpenQuestion holds

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LicenceCC BY-NC
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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.