Evidence map›Paper›PMID 33908706›Full record

ArticleChemistryOpen2021

One-Pot Synthesis of Asymmetrically Difunctionalized Oligomaltosides by Cyclodextrin Ring Opening.

Matthieu Pélingre, Meriem Smadhi, Abed Bil, Véronique Bonnet, José Kovensky

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in ChemistryOpen, 2021. 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. Review
  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

5 authors.

Matthieu PélingreLaboratoire de Glycochimie, des Antimicrobiens et des Agroressources (LG2A), CNRS UMR 7378, Université de Picardie Jules Verne, 33 rue Saint Leu, 80039, Amiens, France.
Meriem SmadhiLaboratoire de Glycochimie, des Antimicrobiens et des Agroressources (LG2A), CNRS UMR 7378, Université de Picardie Jules Verne, 33 rue Saint Leu, 80039, Amiens, France.
Abed BilLaboratoire de Glycochimie, des Antimicrobiens et des Agroressources (LG2A), CNRS UMR 7378, Université de Picardie Jules Verne, 33 rue Saint Leu, 80039, Amiens, France.
Véronique BonnetLaboratoire de Glycochimie, des Antimicrobiens et des Agroressources (LG2A), CNRS UMR 7378, Université de Picardie Jules Verne, 33 rue Saint Leu, 80039, Amiens, France.ORCID 0000-0002-4220-9617
José KovenskyLaboratoire de Glycochimie, des Antimicrobiens et des Agroressources (LG2A), CNRS UMR 7378, Université de Picardie Jules Verne, 33 rue Saint Leu, 80039, Amiens, France.ORCID 0000-0002-6398-2721

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The synthesis of pure difunctionalized hexa-, hepta- and octamaltosides was performed by one-pot chemical reaction from perbenzoylated cyclodextrin. Oligomaltosides with azide, propargyl or allyl on reducing end and an unprotected hydroxyl group on non-reducing end were obtained from perbenzoylated α-, β- and γ-cyclodextrin with 12 to 48 % yields.

Indexed as

AllylationAzidationCyclodextrin ring-openingFunctionalizationOligomaltosides synthesisPropargylation

Identifiers

PMID33908706
PMCPMC8080284

What OpenQuestion holds

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LicenceCC BY-NC
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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.