Evidence map›Paper›PMID 40944370›Full record

ReviewAngewandte Chemie (International ed. in English)2025

Catalytic Strategies for Stereoselective Carbohydrate Synthesis: Emerging Concepts for Accessing Challenging Glycosides.

Charles C J Loh

Abstract readReview
In one paragraph

Review in Angewandte Chemie (International ed. in English), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Site-Selective Distal Arylation of Sugars Enabled by Cyclic Acetals.Journal of the American Chemical Society · 2026
    Article
  4. Article
  5. Article
  6. 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

1 author.

Charles C J LohUCD School of Chemistry, University College Dublin, Belfield, Dublin, 4, Ireland.ORCID 0000-0001-6970-1989

Funding

Boehringer Ingelheim FoundationFonds der Chemischen Industrie Li 198/04
6 · The paper itself

Abstract

The development of innovative catalytic strategies for stereoselective carbohydrate synthesis is rapidly emerging as a theme of general synthetic interest. This research frontier is fuelled by current realization that anomeric and site-selectivity challenges encountered in carbohydrate chemistry are indeed fascinating fundamental synthetic questions, still yet to be satisfactorily addressed. Although specialist carbohydrate chemistry and catalysis developed largely independently over the past three decades, growing recognition of carbohydrates as an excellent platform for catalytic method development is now generating fresh opportunities to advance our understanding of chemical phenomena. Unexpected catalytic mechanisms are often unearthed in such cross-disciplinary endeavours. Moreover, new bond-forming catalytic solutions are in great demand as the definition of biologically relevant glycosidic chemical space has broadened substantially beyond native oligosaccharides to include glycomimetics, rare and non-classical sugars. Distinctly, the last 5 years is marked by an unprecedented flurry of activity in the development of ground-breaking catalytic carbohydrate transformations, leading to robust methods that diverge from classical glycosylation approaches. In this minireview, lately emerging concepts such as noncovalent catalyzed glycosylations, radical catalyzed glycosylations, asymmetric catalytic carbohydrate functionalizations and new glycosylation modalities will be examined.

Indexed as

CarbohydratesGlycosidesCatalysisGlycosylationStereoisomerismCarbohydratesGlycosidesCarbohydratesCatalysisGlycosylationNoncovalent interactionsStereoselectivity

Identifiers

PMID40944370
PMCPMC12518707

What Socratic 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 Socratic graph.