Evidence map›Paper›PMID 35286004›Full record

ArticleAngewandte Chemie (International ed. in English)2022

Mesoionic Imines (MIIs): Strong Donors and Versatile Ligands for Transition Metals and Main Group Substrates.

Richard Rudolf, Nicolás I Neuman, Robert R M Walter, Mark R Ringenberg, Biprajit Sarkar

Open access · hybridAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

4 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
  2. Article
  3. PPhAngewandte Chemie (International ed. in English) · 2025
    Article
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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

5 authors at 1 institution in 2 countries.

Richard RudolfLehrstuhl für Anorganische Koordinationschemie, Institut für Anorganische Chemie, University of Stuttgart, Pfaffenwaldring 55, 70569, Stuttgart, Germany.
Nicolás I NeumanLehrstuhl für Anorganische Koordinationschemie, Institut für Anorganische Chemie, University of Stuttgart, Pfaffenwaldring 55, 70569, Stuttgart, Germany.ORCID http://orcid.org/0000-0003-3368-0228
Robert R M WalterLehrstuhl für Anorganische Koordinationschemie, Institut für Anorganische Chemie, University of Stuttgart, Pfaffenwaldring 55, 70569, Stuttgart, Germany.
Mark R RingenbergLehrstuhl für Anorganische Koordinationschemie, Institut für Anorganische Chemie, University of Stuttgart, Pfaffenwaldring 55, 70569, Stuttgart, Germany.
Biprajit SarkarLehrstuhl für Anorganische Koordinationschemie, Institut für Anorganische Chemie, University of Stuttgart, Pfaffenwaldring 55, 70569, Stuttgart, Germany.ORCID http://orcid.org/0000-0003-4887-7277
University of Stuttgart · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report the synthesis and the reactivity of 1,2,3-triazolin-5-imine type mesoionic imines (MIIs). The MIIs are accessible by a base-mediated cycloaddition between a substituted acetonitrile and an aromatic azide, methylation by established routes and subsequent deprotonation. C=O-stretching frequencies in MII-CO

Indexed as

C−H ActivationElectronic AmbivalenceFluorine Specific InteractionsMesoionic IminesStrong Donors

Identifiers

PMID35286004
PMCPMC9322014
OpenAlexW4220777908

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.