Evidence map›Paper›PMID 37306545›Full record

ArticleChemistry (Weinheim an der Bergstrasse, Germany)2023

Cyclotrimerization Approach to Symmetric [9]Helical Indenofluorenes: Diverting Cyclization Pathways.

Timothée Cadart, Tim Gläsel, Ivana Císařová, Róbert Gyepes, David Nečas, Marko Hapke, Martin Kotora

Open access · hybridAbstract read
In one paragraph

Article in Chemistry (Weinheim an der Bergstrasse, Germany), 2023. 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
0.9field-weighted citation impact, top 30% of its field
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, 6 citations in OpenAlex.

  1. Helical Dispiroindeno[2,1-The Journal of organic chemistry · 2026
    Article
  2. 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

7 authors at 3 institutions in 2 countries.

Timothée CadartDepartment of Organic Chemistry, Faculty of Science, Charles University in Prague, Hlavova 8, 128 43, Praha 2, Czech Republic.ORCID https://orcid.org/0000-0002-7806-5483
Tim GläselInstitute for Catalysis (INCA), Johannes Kepler University Linz, Altenberger Strasse 69, A-4040, Linz, Austria.
Ivana CísařováDepartment of Inorganic Chemistry, Faculty of Science, Charles University in Prague, Hlavova 8, 128 43, Praha 2, Czech Republic.ORCID https://orcid.org/0000-0002-9612-9831
Róbert GyepesDepartment of Molecular Electrochemistry and Catalysis, J. Heyrovský Institute of Physical Chemistry of the Czech Academy of Sciences, Dolejškova, 2155/3, 182 23, Praha 8, Czech Republic.ORCID https://orcid.org/0000-0002-2908-0425
David NečasDepartment of Organic Chemistry, Faculty of Science, Charles University in Prague, Hlavova 8, 128 43, Praha 2, Czech Republic.ORCID https://orcid.org/0000-0001-6255-0954
Marko HapkeInstitute for Catalysis (INCA), Johannes Kepler University Linz, Altenberger Strasse 69, A-4040, Linz, Austria.ORCID https://orcid.org/0000-0001-7454-9184
Martin KotoraDepartment of Organic Chemistry, Faculty of Science, Charles University in Prague, Hlavova 8, 128 43, Praha 2, Czech Republic.ORCID https://orcid.org/0000-0003-4491-7091
Charles University · CZJohannes Kepler University of Linz · ATCzech Academy of Sciences, J. Heyrovský Institute of Physical Chemistry · CZ

Funding

Austrian Science Fund I 5385Grantová Agentura České Republiky 21-39639LUniverzita Karlova v Praze UNCE/SCI/014
6 · The paper itself

Abstract

Catalytic cyclotrimerization routes to symmetrical [9]helical indenofluorene were explored by using different transition-metal complexes and thermal conditions. Depending on the reaction conditions, the cyclotrimerizations were accompanied by dehydro-Diels-Alder reaction giving rise to another type of aromatic compounds. Structures of both symmetrical [9]helical cyclotrimerization product as well as the dehydro-Diels-Alder product were confirmed by single-crystal X-ray diffraction analyses. Limits of enantioselective cyclotrimerization were assessed as well. DFT calculations shed light on the reaction course and the origin of diminished enantioselectivity.

Indexed as

[9]helical structurecatalysisC−C bond cleavagecyclotrimerizationdispiroindenofluorenes

Identifiers

PMID37306545
PMCPMC10946996
OpenAlexW4380291582

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.