Evidence mapPaperPMID 42380139Full record

ArticleNature communications2026

Carbene-catalyzed site-selective sulfonylation and modular edition of monosaccharides for hydroxyl group stereoinversion and swapping.

Hongyan Long, Gangyu Wang, Chunyan Jian, Luhang Yang, Xingxing Wu, Yonggui Robin Chi

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Hongyan LongState Key Laboratory of Green Pesticide; Center for R&D of Fine Chemicals of Guizhou University, Huaxi District, Guiyang, China.
Gangyu WangState Key Laboratory of Green Pesticide; Center for R&D of Fine Chemicals of Guizhou University, Huaxi District, Guiyang, China.
Chunyan JianState Key Laboratory of Green Pesticide; Center for R&D of Fine Chemicals of Guizhou University, Huaxi District, Guiyang, China.
Luhang YangState Key Laboratory of Green Pesticide; Center for R&D of Fine Chemicals of Guizhou University, Huaxi District, Guiyang, China.
Xingxing WuState Key Laboratory of Green Pesticide; Center for R&D of Fine Chemicals of Guizhou University, Huaxi District, Guiyang, China. wuxx@gzu.edu.cn.ORCID http://orcid.org/0000-0002-6281-243X
Yonggui Robin ChiState Key Laboratory of Green Pesticide; Center for R&D of Fine Chemicals of Guizhou University, Huaxi District, Guiyang, China. robinchi@ntu.edu.sg.ORCID http://orcid.org/0000-0003-0573-257X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Monosaccharides are ubiquitous motifs in natural and synthetic molecules, yet methods for their selective structure editing remain limited due to the multiple hydroxy groups for differentiation and their structural complexity. Among possible strategies for stereoinversion and functional group swapping of saccharides, the classical S

Indexed as

MethaneMonosaccharidesCatalysisStereoisomerismcarbeneMethaneMonosaccharides

Identifiers

PMID42380139
PMCPMC13458833

What Socratic 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 Socratic graph.