Evidence map›Paper›PMID 41163828›Full record

ArticleRSC advances2025

Synthesis of azulenyl-substituted gold(i)-carbene complexes and investigation of their anticancer activity.

Martin C Dietl, Christopher Hüßler, Matthias Scherr, Zoé M Frederiksen, Jürgen Graf, Frank Rominger, Matthias Rudolph, Isabella Caligiuri, Laura Tripodi, Flavio Rizzolio and 2 more

Abstract read
In one paragraph

Article in RSC advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Martin C DietlOrganisch-Chemisches Institut, Heidelberg University Im Neuenheimer Feld 270 69120 Heidelberg Germany hashmi@hashmi.de http://www.hashmi.de (+49)-6221-54-4205.ORCID https://orcid.org/0000-0002-6115-4674
Christopher HüßlerOrganisch-Chemisches Institut, Heidelberg University Im Neuenheimer Feld 270 69120 Heidelberg Germany hashmi@hashmi.de http://www.hashmi.de (+49)-6221-54-4205.ORCID https://orcid.org/0009-0000-5716-8814
Matthias ScherrOrganisch-Chemisches Institut, Heidelberg University Im Neuenheimer Feld 270 69120 Heidelberg Germany hashmi@hashmi.de http://www.hashmi.de (+49)-6221-54-4205.ORCID https://orcid.org/0009-0000-4548-9741
Zoé M FrederiksenOrganisch-Chemisches Institut, Heidelberg University Im Neuenheimer Feld 270 69120 Heidelberg Germany hashmi@hashmi.de http://www.hashmi.de (+49)-6221-54-4205.ORCID https://orcid.org/0009-0005-9777-1083
Jürgen GrafOrganisch-Chemisches Institut, Heidelberg University Im Neuenheimer Feld 270 69120 Heidelberg Germany hashmi@hashmi.de http://www.hashmi.de (+49)-6221-54-4205.ORCID https://orcid.org/0000-0002-9107-4843
Frank RomingerOrganisch-Chemisches Institut, Heidelberg University Im Neuenheimer Feld 270 69120 Heidelberg Germany hashmi@hashmi.de http://www.hashmi.de (+49)-6221-54-4205.
Matthias RudolphOrganisch-Chemisches Institut, Heidelberg University Im Neuenheimer Feld 270 69120 Heidelberg Germany hashmi@hashmi.de http://www.hashmi.de (+49)-6221-54-4205.
Isabella CaligiuriPathology Unit, Department of Molecular Biology and Translational Research, Centro di Riferimento Oncologico di Aviano (CRO), IRCCS Via Franco Gallini 2 33081 Aviano Italy.
Laura TripodiDipartimento di Scienze Molecolari e Nanosistemi, Università Ca' Foscari Campus Scientifico Via Torino 155 30174 Venezia-Mestre Italy.
Flavio RizzolioPathology Unit, Department of Molecular Biology and Translational Research, Centro di Riferimento Oncologico di Aviano (CRO), IRCCS Via Franco Gallini 2 33081 Aviano Italy.ORCID https://orcid.org/0000-0002-3400-4363
Thomas ScattolinDipartimento di Scienze Chimiche, Università Degli Studi di Padova Via Marzolo 1 35131 Padova Italy thomas.scattolin@unipd.it.ORCID https://orcid.org/0000-0001-7345-9670
A Stephen K HashmiOrganisch-Chemisches Institut, Heidelberg University Im Neuenheimer Feld 270 69120 Heidelberg Germany hashmi@hashmi.de http://www.hashmi.de (+49)-6221-54-4205.ORCID https://orcid.org/0000-0002-6720-8602

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The direct and atom economic synthesis of azulenyl-substituted gold(i) carbene complexes, based on the modular template synthesis using gold(i) isonitrile complexes and amine nucleophiles, is presented. First, two azulenyl-substituted isonitriles as ligands were synthesized from a functionalizable azulene derivative, the latter stemming from a gold-catalyzed dimerization of internal alkynes. These azulene-bound gold(i) isonitrile complexes allow the smooth nucleophilic attack by both aliphatic and aromatic amines. The newly synthesized azulene-substituted gold(i) carbene complexes were evaluated for

Identifiers

PMID41163828
PMCPMC12560230

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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.