Evidence map›Paper›PMID 40561111›Full record

ArticleChemistry (Weinheim an der Bergstrasse, Germany)2025

Nucleophilic Addition versus Migratory Insertion Pathways in the Gold-Catalyzed Heck Reaction: A Computational Study.

Peter H M Budzelaar, Luca Rocchigiani, Manfred Bochmann

Abstract read
In one paragraph

Article in Chemistry (Weinheim an der Bergstrasse, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. TheBeilstein journal of organic chemistry · 2026
    Article
  2. StereoselectiveACS organic & inorganic Au · 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

3 authors.

Peter H M BudzelaarDepartment of Chemistry, University of Naples Federico II, Via Cintia, Naples, I-80126, Italy.ORCID https://orcid.org/0000-0003-0039-4479
Luca RocchigianiDepartment of Chemistry, Biology and Biotechnology, University of Perugia, Via Elce di Sotto 8, Perugia, I-06134, Italy.ORCID https://orcid.org/0000-0002-2679-8407
Manfred BochmannSchool of Chemistry, University of East Anglia, Norwich Research Park, Norwich, NR4 7TJ, UK.ORCID https://orcid.org/0000-0001-7736-5428

Funding

HORIZON EUROPE European Innovation Ecosystems ECS00000041-VITALITYLeverhulme Trust EM-2024-028∖4Royal Society of Chemistry R22-0875640255
6 · The paper itself

Abstract

The initial reaction steps in the formation of Heck-type arylated alkenes catalyzed by P^N chelated Au(III) complexes have been studied computationally. Two mechanistic alternatives have been explored: (1) alkene coordination and insertion into a gold-carbon bond, and (2) nucleophilic attack on a gold(III) alkene adduct. The common starting point, the [(P^N)AuPh(alkene)]

Indexed as

catalysischelate ligandsDFTgoldmechanisms

Identifiers

PMID40561111
PMCPMC12284628

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.