Evidence map›Paper›PMID 31529676›Full record

ArticleAngewandte Chemie (International ed. in English)2019

Carboamination of Unactivated Alkenes through Three-Component Radical Conjugate Addition.

Heng Jiang, Gesa Seidler, Armido Studer

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. Nickel-Catalyzed Twofold Conjunctive Coupling via Philicity-Alternating Radical Relay.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  2. Article
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  4. Aminoalkylation of Alkenes Enabled by Triple Radical Sorting.Journal of the American Chemical Society · 2025
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  19. Exploiting Imine Photochemistry for Masked N-Centered Radical Reactivity.Angewandte Chemie (International ed. in English) · 2019
    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

3 authors.

Heng JiangOrganisch-Chemisches Institut, Westfälische Wilhelms-Universität, Corrensstraß 40, 48149, Münster, Germany.
Gesa SeidlerOrganisch-Chemisches Institut, Westfälische Wilhelms-Universität, Corrensstraß 40, 48149, Münster, Germany.
Armido StuderOrganisch-Chemisches Institut, Westfälische Wilhelms-Universität, Corrensstraß 40, 48149, Münster, Germany.ORCID 0000-0002-1706-513X

Funding

H2020 European Research Council ERC Advanced Grant agreement No.692640
6 · The paper itself

Abstract

Two-component Giese type radical additions are highly practical and established reactions. Herein, three-component radical conjugate additions of unactivated alkenes to Michael acceptors are reported. Amidyl radicals, oxidatively generated from α-amido oxy acids using redox catalysis, act as the third reaction component which add to the unactivated alkenes. The adduct radicals engage in Giese type additions to Michael acceptors to provide, after reduction, the three-component products in an overall alkene carboamination reaction. Transformations which can be conducted under practical mild conditions feature high functional group tolerance and broad substrate scope.

Indexed as

amidyl radicalscarboamination of alkenesGiese reactionphotoredox catalysisradical cascade

Identifiers

PMID31529676
PMCPMC6900080

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.