Evidence map›Paper›PMID 39055149›Full record

ArticleJACS Au2024

Domino Conjugate Addition-1,4-Aryl Migration for the Synthesis of α,β-Difunctionalized Amides.

Haoqi Zhang, Yi Xiao, Miran Lemmerer, Tommaso Bortolato, Nuno Maulide

Abstract read
In one paragraph

Article in JACS Au, 2024. 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. Article
  2. Article
  3. Smiles-Truce Cascades Enable Heteroaryl Cyclopropane and Sultine Synthesis.Angewandte Chemie (International ed. in English) · 2025
    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

5 authors.

Haoqi ZhangInstitute of Organic Chemistry, University of Vienna, Währinger Straße 38, 1090 Vienna, Austria.
Yi XiaoInstitute of Organic Chemistry, University of Vienna, Währinger Straße 38, 1090 Vienna, Austria.
Miran LemmererInstitute of Organic Chemistry, University of Vienna, Währinger Straße 38, 1090 Vienna, Austria.ORCID https://orcid.org/0000-0003-4391-055X
Tommaso BortolatoInstitute of Organic Chemistry, University of Vienna, Währinger Straße 38, 1090 Vienna, Austria.
Nuno MaulideInstitute of Organic Chemistry, University of Vienna, Währinger Straße 38, 1090 Vienna, Austria.ORCID https://orcid.org/0000-0003-3643-0718

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A domino difunctionalization of sulfonyl(acryl)imides to form β-substituted α-aryl amides is reported. This transformation involves a 1,4-addition followed by a polar Truce-Smiles rearrangement process, entropically driven by release of SO

Identifiers

PMID39055149
PMCPMC11267538

What OpenQuestion holds

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Registered trials

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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.