Evidence map›Paper›PMID 33930267›Full record

ReviewAccounts of chemical research2021

Glycosyl Oxocarbenium Ions: Structure, Conformation, Reactivity, and Interactions.

Antonio Franconetti, Ana Ardá, Juan Luis Asensio, Yves Blériot, Sébastien Thibaudeau, Jesús Jiménez-Barbero

Abstract readReview
In one paragraph

Review in Accounts of chemical research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing 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

42 citing papers in PubMed.

  1. Article
  2. Stereoselectivity of Galactosylation Reactions In Vacuo.Journal of the American Chemical Society · 2026
    Article
  3. Article
  4. Anomer-Selective Vorbrüggen Reaction for the Catalytic Synthesis of CJournal of the American Chemical Society · 2026
    Article
  5. Article
  6. Article
  7. Confined Acids Catalyze a Broadly Applicable β-SelectiveJournal of the American Chemical Society · 2026
    Article
  8. Article
  9. Elucidating the Stereodirecting Effect of C-4 Acyl Groups on Galactosyl Donors.Angewandte Chemie (International ed. in English) · 2026
    Article
  10. Article
  11. The Formation of Covalent Linkages in Lignocellulosic Biomass via the Oxocarbenium Intermediate.Chemphyschem : a European journal of chemical physics and physical chemistry · 2026
    Article
  12. Article
  13. Nanozymes Integrated Biochips Toward Smart Detection System.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  14. Article
  15. Article
  16. Mechanism of 3-The Journal of organic chemistry · 2025
    Article
  17. Article
  18. Review
  19. Article
  20. 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.

Antonio FranconettiCIC bioGUNE, Basque Research and Technology Alliance (BRTA), Bizkaia Technology Park, Building 800, 48160 Derio, Spain.ORCID 0000-0002-7972-8795
Ana ArdáCIC bioGUNE, Basque Research and Technology Alliance (BRTA), Bizkaia Technology Park, Building 800, 48160 Derio, Spain.ORCID 0000-0003-3027-7417
Juan Luis AsensioInstituto de Química Orgánica (IQOG-CSIC), Juan de la Cierva 3, 28006 Madrid, Spain.ORCID 0000-0001-7536-5221
Yves BlériotUniversité de Poitiers, IC2MP, UMR CNRS 7285, Equipe "OrgaSynth", 4 rue Michel Brunet, 86073 cedex 9 Poitiers, France.ORCID 0000-0002-3209-9282
Sébastien ThibaudeauUniversité de Poitiers, IC2MP, UMR CNRS 7285, Equipe "OrgaSynth", 4 rue Michel Brunet, 86073 cedex 9 Poitiers, France.ORCID 0000-0002-6246-5829
Jesús Jiménez-BarberoCIC bioGUNE, Basque Research and Technology Alliance (BRTA), Bizkaia Technology Park, Building 800, 48160 Derio, Spain.ORCID 0000-0001-5421-8513

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Carbohydrates (glycans, saccharides, and sugars) are essential molecules in all domains of life. Research on glycoscience spans from chemistry to biomedicine, including material science and biotechnology. Access to pure and well-defined complex glycans using synthetic methods depends on the success of the employed glycosylation reaction. In most cases, the mechanism of the glycosylation reaction is believed to involve the oxocarbenium ion. Understanding the structure, conformation, reactivity, and interactions of this glycosyl cation is essential to predict the outcome of the reaction. In this Account, building on our contributions on this topic, we discuss the theoretical and experimental approaches that have been employed to decipher the key features of glycosyl cations, from their structures to their interactions and reactivity.We also highlight that, from a chemical perspective, the glycosylation reaction can be described as a continuum, from unimolecular S

Indexed as

GlycosylationIonsMethaneModels, MolecularMolecular ConformationcarbeneIonsMethane

Identifiers

PMID33930267
PMCPMC8173606

What OpenQuestion holds

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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.