Evidence map›Paper›PMID 37416699›Full record

ArticleChemical science2023

Self-assembly of achiral building blocks into chiral cyclophanes using non-directional interactions.

Yuan Zhang, Benjamin Ourri, Pierre-Thomas Skowron, Emeric Jeamet, Titouan Chetot, Christian Duchamp, Ana M Belenguer, Nicolas Vanthuyne, Olivier Cala, Elise Dumont and 5 more

Abstract read
In one paragraph

Article in Chemical science, 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
–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. Article
  2. Dynamic covalent synthesis.Chemical science · 2024
    Review
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

15 authors.

Yuan ZhangAix Marseille Univ, CNRS, Centrale Marseille, iSm2 Marseille France.
Benjamin OurriUniv Lyon, Univ Lyon 1, CNRS, INSA, CPE, ICBMS F-69622 Lyon France laurent.vial@univ-lyon1.fr julien.leclaire@univ-lyon1.fr.ORCID https://orcid.org/0000-0002-0250-366X
Pierre-Thomas SkowronAix Marseille Univ, CNRS, Centrale Marseille, iSm2 Marseille France.
Emeric JeametUniv Lyon, Univ Lyon 1, CNRS, INSA, CPE, ICBMS F-69622 Lyon France laurent.vial@univ-lyon1.fr julien.leclaire@univ-lyon1.fr.
Titouan ChetotUniv Lyon, Univ Lyon 1, CNRS, INSA, CPE, ICBMS F-69622 Lyon France laurent.vial@univ-lyon1.fr julien.leclaire@univ-lyon1.fr.
Christian DuchampUniv Lyon, Univ Lyon 1, CNRS, INSA, CPE, ICBMS F-69622 Lyon France laurent.vial@univ-lyon1.fr julien.leclaire@univ-lyon1.fr.
Ana M BelenguerYusuf Hamied Department of Chemistry, University of Cambridge Lensfield Road Cambridge CB2 1EW UK.ORCID https://orcid.org/0000-0002-0443-4856
Nicolas VanthuyneAix Marseille Univ, CNRS, Centrale Marseille, iSm2 Marseille France.ORCID https://orcid.org/0000-0003-2598-7940
Olivier CalaInstitut des Sciences Analytiques, UMR 5280 CNRS, Université Claude Bernard Lyon Lyon France.ORCID https://orcid.org/0000-0003-3579-0973
Elise DumontENSL, CNRS, Laboratoire de Chimie UMR 5182 46 allée d'Italie 69364 Lyon France.ORCID https://orcid.org/0000-0002-2359-111X
Pradeep K MandalDepartment of Pharmacy and Center for Integrated Protein Science, Ludwig-Maximilians-Universität Butenandtstr., 5-13 81377 München Germany.ORCID https://orcid.org/0000-0001-5996-956X
Ivan HucDepartment of Pharmacy and Center for Integrated Protein Science, Ludwig-Maximilians-Universität Butenandtstr., 5-13 81377 München Germany.ORCID https://orcid.org/0000-0001-7036-9696
Florent PerretUniv Lyon, Univ Lyon 1, CNRS, INSA, CPE, ICBMS F-69622 Lyon France laurent.vial@univ-lyon1.fr julien.leclaire@univ-lyon1.fr.
Laurent VialUniv Lyon, Univ Lyon 1, CNRS, INSA, CPE, ICBMS F-69622 Lyon France laurent.vial@univ-lyon1.fr julien.leclaire@univ-lyon1.fr.ORCID https://orcid.org/0000-0002-0357-0573
Julien LeclaireUniv Lyon, Univ Lyon 1, CNRS, INSA, CPE, ICBMS F-69622 Lyon France laurent.vial@univ-lyon1.fr julien.leclaire@univ-lyon1.fr.ORCID https://orcid.org/0000-0001-7984-9055

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The diastereoselective assembly of achiral constituents through a single spontaneous process into complex covalent architectures bearing multiple stereogenic elements still remains a challenge for synthetic chemists. Here, we show that such an extreme level of control can be achieved by implementing stereo-electronic information on synthetic organic building blocks and templates and that non-directional interactions (

Identifiers

PMID37416699
PMCPMC10321575

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.