Evidence map›Paper›PMID 32181544›Full record

ArticleChemistry (Weinheim an der Bergstrasse, Germany)2020

Facile Synthesis of a Stable Side-on Phosphinyne Complex by Redox Driven Intramolecular Cyclisation.

Helge Lange, Henning Schröder, Elisabeth Oberem, Alexander Villinger, Jabor Rabeah, Ralf Ludwig, Klaus Neymeyr, Wolfram W Seidel

Abstract read
In one paragraph

Article in Chemistry (Weinheim an der Bergstrasse, Germany), 2020. 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. 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

8 authors.

Helge LangeInstitut für Chemie, Universität Rostock, Albert-Einstein-Str. 3a, 18059, Rostock, Germany.
Henning SchröderInstitut für Mathematik, Universität Rostock, Ulmenstraße 69, 18057, Rostock, Germany.
Elisabeth OberemInstitut für Chemie, Universität Rostock, Albert-Einstein-Str. 3a, 18059, Rostock, Germany.
Alexander VillingerInstitut für Chemie, Universität Rostock, Albert-Einstein-Str. 3a, 18059, Rostock, Germany.ORCID http://orcid.org/0000-0002-0868-9987
Jabor RabeahLeibniz-Institut für Katalyse e.V., Albert-Einstein-Straße 29a, 18059, Rostock, Germany.ORCID http://orcid.org/0000-0003-2162-0981
Ralf LudwigInstitut für Chemie, Universität Rostock, Albert-Einstein-Str. 3a, 18059, Rostock, Germany.
Klaus NeymeyrInstitut für Mathematik, Universität Rostock, Ulmenstraße 69, 18057, Rostock, Germany.ORCID http://orcid.org/0000-0002-1464-2851
Wolfram W SeidelInstitut für Chemie, Universität Rostock, Albert-Einstein-Str. 3a, 18059, Rostock, Germany.ORCID http://orcid.org/0000-0003-1891-361X

Funding

Deutsche Forschungsgemeinschaft SE 890/7-1
6 · The paper itself

Abstract

Alkyne complexes with vicinal substitution by a Lewis acid and a Lewis base at the coordinated alkyne are prospective frustrated Lewis pairs exhibiting a particular mutual distance and, hence, a specific activation potential. In this contribution, investigations on the generation of a W

Indexed as

alkyne complexcyclisation mechanismfrustrated Lewis pairnon-innocent ligandphosphinyne complex

Identifiers

PMID32181544
PMCPMC7540294

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.