Evidence map›Paper›PMID 35493246›Full record

ArticleRSC advances2021

Metal-free catalytic hydrocarboxylation of hexafluorobut-2-yne.

Ji-Jun Zeng, Bo Zhao, Xiao-Bo Tang, Sheng Han, Zhi-Qiang Yang, Ze-Peng Liu, Wei Zhang, Jian Lu

Open access · goldAbstract read
In one paragraph

Article in RSC advances, 2021. 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, top 84% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

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

8 authors.

Ji-Jun ZengState Key Laboratory of Fluorine & Nitrogen Chemicals, Xi'an Modern Chemistry Research Institute Xi'an 710065 China lujian204@263.net Zhangwei_204@163.com.ORCID https://orcid.org/0000-0003-4426-2021
Bo ZhaoState Key Laboratory of Fluorine & Nitrogen Chemicals, Xi'an Modern Chemistry Research Institute Xi'an 710065 China lujian204@263.net Zhangwei_204@163.com.
Xiao-Bo TangState Key Laboratory of Fluorine & Nitrogen Chemicals, Xi'an Modern Chemistry Research Institute Xi'an 710065 China lujian204@263.net Zhangwei_204@163.com.
Sheng HanState Key Laboratory of Fluorine & Nitrogen Chemicals, Xi'an Modern Chemistry Research Institute Xi'an 710065 China lujian204@263.net Zhangwei_204@163.com.
Zhi-Qiang YangState Key Laboratory of Fluorine & Nitrogen Chemicals, Xi'an Modern Chemistry Research Institute Xi'an 710065 China lujian204@263.net Zhangwei_204@163.com.
Ze-Peng LiuState Key Laboratory of Fluorine & Nitrogen Chemicals, Xi'an Modern Chemistry Research Institute Xi'an 710065 China lujian204@263.net Zhangwei_204@163.com.
Wei ZhangState Key Laboratory of Fluorine & Nitrogen Chemicals, Xi'an Modern Chemistry Research Institute Xi'an 710065 China lujian204@263.net Zhangwei_204@163.com.
Jian LuState Key Laboratory of Fluorine & Nitrogen Chemicals, Xi'an Modern Chemistry Research Institute Xi'an 710065 China lujian204@263.net Zhangwei_204@163.com.ORCID https://orcid.org/0000-0002-0494-2498

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An efficient method for stereoselective synthesis of trifluorinated enol esters catalyzed by base was introduced. The DFT calculations and experimental results both supported the nucleophilic addition process. The protocol featured mild reaction conditions and showed a wide functional group tolerance. The one-pot simultaneous etherification and esterification of the salicylic acids further demonstrated the prospective synthetic application.

Identifiers

PMID35493246
PMCPMC9044190
OpenAlexW4205166330

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.