Evidence map›Paper›PMID 41230956›Full record

ArticleAngewandte Chemie (International ed. in English)2026

Enhanced Selectivity of Chalcogen Bonding over Halogen Bonding Catalyzed C-glycosylation Through Differentiated Intermediate Activation.

Hao Guo, Charles C J Loh

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. 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

2 authors.

Hao GuoCollege of Chemistry and Materials Science, Guangdong Provincial Key Laboratory of Functional Supramolecular Coordination Materials and Applications, Jinan University, Guangzhou, 510632, P.R. China.
Charles C J LohUCD School of Chemistry, University College Dublin, Belfield, Dublin 4, Dublin, Ireland.ORCID https://orcid.org/0000-0001-6970-1989

Funding

Boehringer Ingelheim StiftungDeutsche Forschungsgemeinschaft 452669688Fonds der Chemischen Industrie Li198/04
6 · The paper itself

Abstract

σ-hole-based noncovalent interactions are gaining intense attention as robust tools in stereoselective carbohydrate synthesis. However, the mechanistic understanding behind the differing performance between chalcogen bonding (ChB) catalysis versus halogen bonding (XB) catalysis in chemical glycosylations still remains unresolved. Herein, we disclose a remarkable instance whereby phosphonochalcogenide (PCH) catalysis displays pronounced selectivity and reactivity elevation in aryl-C-glycosylations compared to XB catalysis. Mechanistic studies revealed that the enhanced stereocontrol can be attributed to the differentiated downstream activation of a key bicyclic intermediate. Hammett analysis supported that ChB catalysis shifted the C-glycosylation toward the S

Indexed as

Chalcogen bondingGlycosylationNoncovalent interactionsOrganocatalysisReaction mechanisms

Identifiers

PMID41230956
PMCPMC12790375

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.