Evidence map›Paper›PMID 35222931›Full record

ArticleChemical science2022

α-Diimine synthesis

Connor W Frye, Dominic T Egger, Errikos Kounalis, Adam J Pearce, Yukun Cheng, Ian A Tonks

Abstract read
In one paragraph

Article in Chemical science, 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
–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

4 citing papers in PubMed.

  1. 1,2-Dihydropyrimidine synthesisChemical communications (Cambridge, England) · 2025
    Article
  2. Article
  3. Review
  4. 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

6 authors.

Connor W FryeDepartment of Chemistry, University of Minnesota - Twin Cities 207 Pleasant St SE Minneapolis Minnesota 55455 USA itonks@umn.edu.ORCID https://orcid.org/0000-0002-1985-6365
Dominic T EggerDepartment of Chemistry, University of Minnesota - Twin Cities 207 Pleasant St SE Minneapolis Minnesota 55455 USA itonks@umn.edu.ORCID https://orcid.org/0000-0002-5143-199X
Errikos KounalisDepartment of Chemistry, University of Minnesota - Twin Cities 207 Pleasant St SE Minneapolis Minnesota 55455 USA itonks@umn.edu.ORCID https://orcid.org/0000-0002-8951-4467
Adam J PearceDepartment of Chemistry, University of Minnesota - Twin Cities 207 Pleasant St SE Minneapolis Minnesota 55455 USA itonks@umn.edu.ORCID https://orcid.org/0000-0003-1068-703X
Yukun ChengDepartment of Chemistry, University of Minnesota - Twin Cities 207 Pleasant St SE Minneapolis Minnesota 55455 USA itonks@umn.edu.ORCID https://orcid.org/0000-0002-2379-9404
Ian A TonksDepartment of Chemistry, University of Minnesota - Twin Cities 207 Pleasant St SE Minneapolis Minnesota 55455 USA itonks@umn.edu.ORCID https://orcid.org/0000-0001-8451-8875

Funding

Ti-Catalyzed Oxidative Amination ReactionsR35GM119457 · NIGMS · UNIVERSITY OF MINNESOTA · PI Ian Albert Tonks · 2016 to 2026
$4.4M
Upgrade of a 500 MHz NMR Spectrometer for Applications in Biomedical ResearchS10OD011952 · OD · UNIVERSITY OF MINNESOTA · PI HOYE, THOMAS R. · 2012 to 2012
$378k
Designing Ligand Platforms of Titanium Imido Catalysts and Statistically Screening Alkyne Substrates for [2+2+1] Regioselective Pyrrole SynthesisF32GM137547 · NIGMS · UNIVERSITY OF MINNESOTA · PI HUH, DANIEL NAMHYUK · 2021 to 2022
$109k
NIGMS NIH HHS F32 GM137547NIGMS NIH HHS R35 GM119457NIH HHS S10 OD011952
6 · The paper itself

Abstract

α-Diimines are commonly used as supporting ligands for a variety of transition metal-catalyzed processes, most notably in α-olefin polymerization. They are also precursors to valuable synthetic targets, such as chiral 1,2-diamines. Their synthesis is usually performed through acid-catalyzed condensation of amines with α-diketones. Despite the simplicity of this approach, accessing unsymmetrical α-diimines is challenging. Herein, we report the Ti-mediated intermolecular diimination of alkynes to afford a variety of symmetrical and unsymmetrical α-diimines through the reaction of diazatitanacyclohexadiene intermediates with C-nitrosos. These diazatitanacycles can be readily accessed

Identifiers

PMID35222931
PMCPMC8809399

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.