Evidence map›Paper›PMID 39560605›Full record

ArticleAngewandte Chemie (International ed. in English)2025

Iodide Anion Enables a Reductive Cross-Electrophile Coupling for Preparing Tertiary Amines.

Miran Lemmerer, Veronica Tona, David Just, Miloš Vavrík, Boris Maryasin, Giovanni Di Mauro, Andreas B Zur Bonsen, Daniel Kaiser, Nuno Maulide

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Eschenmoser's salts: from design to applications in organic synthesis.Organic chemistry frontiers : an international journal of organic chemistry · 2026
    Review
  2. Article
  3. 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

9 authors.

Miran LemmererInstitute of Organic Chemistry, University of Vienna, Währinger Straße 38, 1090, Vienna, Austria.ORCID https://orcid.org/0000-0003-4391-055X
Veronica TonaInstitute of Organic Chemistry, University of Vienna, Währinger Straße 38, 1090, Vienna, Austria.ORCID https://orcid.org/0000-0002-0736-6422
David JustInstitute of Organic Chemistry, University of Vienna, Währinger Straße 38, 1090, Vienna, Austria.ORCID https://orcid.org/0000-0002-9606-9365
Miloš VavríkInstitute of Organic Chemistry, University of Vienna, Währinger Straße 38, 1090, Vienna, Austria.ORCID https://orcid.org/0009-0003-2088-1108
Boris MaryasinInstitute of Organic Chemistry, University of Vienna, Währinger Straße 38, 1090, Vienna, Austria.ORCID https://orcid.org/0000-0001-7943-7333
Giovanni Di MauroInstitute of Organic Chemistry, University of Vienna, Währinger Straße 38, 1090, Vienna, Austria.ORCID https://orcid.org/0000-0002-6123-4543
Andreas B Zur BonsenInstitute of Organic Chemistry, University of Vienna, Währinger Straße 38, 1090, Vienna, Austria.ORCID https://orcid.org/0000-0001-9111-3876
Daniel KaiserInstitute of Organic Chemistry, University of Vienna, Währinger Straße 38, 1090, Vienna, Austria.ORCID https://orcid.org/0000-0001-8895-9969
Nuno MaulideInstitute of Organic Chemistry, University of Vienna, Währinger Straße 38, 1090, Vienna, Austria.ORCID https://orcid.org/0000-0003-3643-0718

Funding

Austrian Science Fund P37182H2020 European Research Council CoG682002University of Vienna uni:docs Fellowship
6 · The paper itself

Abstract

The reducing power of iodide anion is an underexplored property that can be used for the cross-electrophile coupling of organic molecules. Herein we harness this trait for the preparation of tertiary amines through the combination of two simple reagents: an electrophilic-carbon precursor and an iminium iodide in a dual role - both as nitrogen-containing building block and as reducing agent. The underlying mechanism of this new C-C bond-formation paradigm is explored through a combination of experiment and quantum chemical calculations.

Indexed as

cross couplingiminium ioniodideradicalsreaction mechanisms

Identifiers

PMID39560605
PMCPMC11720395

What OpenQuestion holds

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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.