Evidence map›Paper›PMID 29802661›Full record

ArticleChemistry (Weinheim an der Bergstrasse, Germany)2018

A Dipyrrin Programmed for Covalent Loading with Fullerenes.

Chengjie Li, Klaus Wurst, Bernhard Kräutler

Abstract read
In one paragraph

Article in Chemistry (Weinheim an der Bergstrasse, Germany), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. A Dipyrrin Programmed for Covalent Loading with Fullerenes.Chemistry (Weinheim an der Bergstrasse, Germany) · 2018
    Article
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

3 authors.

Chengjie LiInstitute of Organic Chemistry and Centre of Molecular Biosciences, University of Innsbruck, Innrain 80/82, 6020, Innsbruck, Austria.ORCID http://orcid.org/0000-0001-5602-6566
Klaus WurstInstitute of General, Inorganic & Theoretical Chemistry, University of Innsbruck, Innrain 80/82, 6020, Innsbruck, Austria.ORCID http://orcid.org/0000-0002-8774-9051
Bernhard KräutlerInstitute of Organic Chemistry and Centre of Molecular Biosciences, University of Innsbruck, Innrain 80/82, 6020, Innsbruck, Austria.ORCID http://orcid.org/0000-0002-2222-0587

Funding

Fundamental Research Funds for the Central Universities 222201714013National Natural Science Foundation of China 21702062Österreichische Forschungsförderungsgesellschaft I-563 and FWF P-17437Shanghai Pujiang Program 17PJ1401700
6 · The paper itself

Abstract

We describe here a di-(β,β'-sulfoleno)pyrrin programmed for efficient and specific β,β'-functionalization via [4+2] cycloaddition reactions. At 120 °C and in the presence of an excess of C

Indexed as

C60-fullerenecheletropic reactioncycloadditionDiels-Alder reactionsporphyrins

Identifiers

PMID29802661
PMCPMC6099335

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.