Evidence map›Paper›PMID 35424934›Full record

ArticleRSC advances2022

Palladium-catalyzed hydroboration reaction of unactivated alkynes with bis (pinacolato) diboron in water.

Ming Yang, Yunzi Yu, Wenxia Ma, Yuqin Feng, Gang Zhang, Yaqi Wu, Fanyu Zhou, Yongsheng Yang, Dezheng Liu

Abstract read
In one paragraph

Article in RSC advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Ming YangSchool of Chemistry and Engineering, Hubei Key Laboratory of Biomass Fibers and Eco-dyeing & Finishing, Wuhan Textile University 1 Textile Road Wuhan 430073 Hubei China ysyang@wtu.edu.cn.
Yunzi YuSchool of Chemistry and Engineering, Hubei Key Laboratory of Biomass Fibers and Eco-dyeing & Finishing, Wuhan Textile University 1 Textile Road Wuhan 430073 Hubei China ysyang@wtu.edu.cn.
Wenxia MaSchool of Chemistry and Engineering, Hubei Key Laboratory of Biomass Fibers and Eco-dyeing & Finishing, Wuhan Textile University 1 Textile Road Wuhan 430073 Hubei China ysyang@wtu.edu.cn.
Yuqin FengSchool of Chemistry and Engineering, Hubei Key Laboratory of Biomass Fibers and Eco-dyeing & Finishing, Wuhan Textile University 1 Textile Road Wuhan 430073 Hubei China ysyang@wtu.edu.cn.
Gang ZhangSchool of Chemistry and Engineering, Hubei Key Laboratory of Biomass Fibers and Eco-dyeing & Finishing, Wuhan Textile University 1 Textile Road Wuhan 430073 Hubei China ysyang@wtu.edu.cn.
Yaqi WuSchool of Chemistry and Engineering, Hubei Key Laboratory of Biomass Fibers and Eco-dyeing & Finishing, Wuhan Textile University 1 Textile Road Wuhan 430073 Hubei China ysyang@wtu.edu.cn.
Fanyu ZhouSchool of Chemistry and Engineering, Hubei Key Laboratory of Biomass Fibers and Eco-dyeing & Finishing, Wuhan Textile University 1 Textile Road Wuhan 430073 Hubei China ysyang@wtu.edu.cn.
Yongsheng YangSchool of Chemistry and Engineering, Hubei Key Laboratory of Biomass Fibers and Eco-dyeing & Finishing, Wuhan Textile University 1 Textile Road Wuhan 430073 Hubei China ysyang@wtu.edu.cn.ORCID https://orcid.org/0000-0001-6997-4530
Dezheng LiuSchool of Mechanical Engineering, Hubei University of Arts and Science No. 296 Longzhong Road Xiangyang Hubei Province 41053 P. R. China Liudezheng@126.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A highly efficient and mild palladium-catalyzed hydroboration of unactivated internal alkynes in water is described. Both aryl- and alkyl-substituted alkynes proceeded smoothly within the reaction time to afford the desired vinylboronates in moderate to high yields. Bis (pinacolato) diboron was used to afford α- and β-hydroborated products in the presence of HOAc. These reactions showed high reactivities and tolerance, thus providing a promising method for the synthesis of alkenyl boron compounds.

Identifiers

PMID35424934
PMCPMC8961796

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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.