Evidence map›Paper›PMID 29887983›Full record

ArticleChemical science2018

Stabilising fleeting intermediates of stilbene photocyclization with amino-borane functionalisation: the rare isolation of persistent dihydrophenanthrenes and their [1,5] H-shift isomers.

Yong-Gang Shi, Soren K Mellerup, Kang Yuan, Guo-Fei Hu, Francoise Sauriol, Tai Peng, Nan Wang, Pangkuan Chen, Suning Wang

Open access · diamondAbstract read
In one paragraph

Article in Chemical science, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

8 citing papers in PubMed, 43 citations in OpenAlex.

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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

9 authors at 2 institutions in 2 countries.

Yong-Gang ShiBeijing Key Laboratory of Photoelectronic/Electrophotonic Conversion Materials , School of Chemistry , Beijing Institute of Technology , Beijing 100081 , P. R. China.
Soren K MellerupDepartment of Chemistry , Queen's University , Kingston , Ontario K7L 3N6 , Canada . Email: sw17@queensu.ca.
Kang YuanDepartment of Chemistry , Queen's University , Kingston , Ontario K7L 3N6 , Canada . Email: sw17@queensu.ca.
Guo-Fei HuBeijing Key Laboratory of Photoelectronic/Electrophotonic Conversion Materials , School of Chemistry , Beijing Institute of Technology , Beijing 100081 , P. R. China.
Francoise SauriolDepartment of Chemistry , Queen's University , Kingston , Ontario K7L 3N6 , Canada . Email: sw17@queensu.ca.
Tai PengBeijing Key Laboratory of Photoelectronic/Electrophotonic Conversion Materials , School of Chemistry , Beijing Institute of Technology , Beijing 100081 , P. R. China.
Nan WangBeijing Key Laboratory of Photoelectronic/Electrophotonic Conversion Materials , School of Chemistry , Beijing Institute of Technology , Beijing 100081 , P. R. China.
Pangkuan ChenBeijing Key Laboratory of Photoelectronic/Electrophotonic Conversion Materials , School of Chemistry , Beijing Institute of Technology , Beijing 100081 , P. R. China.
Suning WangBeijing Key Laboratory of Photoelectronic/Electrophotonic Conversion Materials , School of Chemistry , Beijing Institute of Technology , Beijing 100081 , P. R. China.ORCID 0000-0003-0889-251X
Beijing Institute of Technology · CNQueen's University · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The key intermediate, 4a,4b-dihydrophenanthrene (DPH), involved in the photocyclization of stilbene and derivatives is known to be unstable, and is therefore poorly characterized/understood. We have found that functionalising stilbenes with NMe

Identifiers

PMID29887983
PMCPMC5946680
OpenAlexW2794508863

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

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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.