Evidence map›Paper›PMID 29997813›Full record

ArticleChemical science2016

Competition-driven selection in covalent dynamic networks and implementation in organic reactional selectivity.

P Kovaříček, A C Meister, K Flídrová, R Cabot, K Kovaříčková, J-M Lehn

Abstract read
In one paragraph

Article in Chemical science, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Aromatic-Carbonyl Interactions as an Emerging Type of Non-Covalent Interactions.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  3. Constitutional adaptation to pChemical science · 2024
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Environmental control programs the emergence of distinct functional ensembles from unconstrained chemical reactions.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  9. Antiparallel Dynamic Covalent Chemistries.Journal of the American Chemical Society · 2017
    Article
  10. 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

6 authors.

P KovaříčekInstitut de Science et d'Ingénierie Supramoléculaires , Université de Strasbourg , 8 allée Gaspard Monge , 67000 Strasbourg , France . Email: lehn@unistra.fr.ORCID 0000-0002-4404-3606
A C MeisterInstitut de Science et d'Ingénierie Supramoléculaires , Université de Strasbourg , 8 allée Gaspard Monge , 67000 Strasbourg , France . Email: lehn@unistra.fr.
K FlídrováInstitut de Science et d'Ingénierie Supramoléculaires , Université de Strasbourg , 8 allée Gaspard Monge , 67000 Strasbourg , France . Email: lehn@unistra.fr.
R CabotInstitut de Science et d'Ingénierie Supramoléculaires , Université de Strasbourg , 8 allée Gaspard Monge , 67000 Strasbourg , France . Email: lehn@unistra.fr.
K KovaříčkováInstitut de Science et d'Ingénierie Supramoléculaires , Université de Strasbourg , 8 allée Gaspard Monge , 67000 Strasbourg , France . Email: lehn@unistra.fr.
J-M LehnInstitut de Science et d'Ingénierie Supramoléculaires , Université de Strasbourg , 8 allée Gaspard Monge , 67000 Strasbourg , France . Email: lehn@unistra.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Competition among reagents in dynamic combinatorial libraries of increased complexity leads to reactional self-sorting (improved regioselectivity) in mixtures of aldehydes and oligoamines. High selectivity of a given library component is transferred to a different reacting component of low selectivity through a network of underlying equilibrating reactions which provide component exchange between all species. The selectivity of various carbonyl compounds in reactions with amines was also assessed towards the formation of defined sequences of residues along oligoamine chains. The approach was further exploited for defining selective dynamic protecting groups (DPGs), based on the reversible linkage between the substrate and the protecting group. They represent an intermediate approach between the conventional protecting groups and the protecting-group-free approach in organic synthesis. Removal of the protecting group is effected

Identifiers

PMID29997813
PMCPMC6005339

What OpenQuestion holds

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LicenceCC BY
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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.