Evidence map›Paper›PMID 42631568›Full record

ReviewChemistry, an Asian journal2026

C─S Bond Metathesis Reactions: Concepts, Scope, and Mechanistic Insight.

Hongmei Liu, Youwei Xie

Abstract readReview
In one paragraph

Review in Chemistry, an Asian journal, 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

2 authors.

Hongmei LiuSchool of Chemistry and Chemical Engineering, Huazhong University of Science and Technology, Wuhan, China.
Youwei XieSchool of Chemistry and Chemical Engineering, Huazhong University of Science and Technology, Wuhan, China.ORCID https://orcid.org/0000-0003-3831-4059

Funding

National Natural Science Foundation of China 22171095
6 · The paper itself

Abstract

Organic sulfides (thioethers) are important building blocks that have widespread applications across various areas. Over the past two decades, tremendous efforts have been dedicated to the development of new and more efficient synthetic protocols for the construction of organic sulfides, among which the sulfide C─S metathesis reaction via a swap of the two bonding groups on the C─S moieties represents an ingenious strategy due to the fact that it allows fast access to synthetically challenging organic sulfides by editing C─S bonds of easily available ones. This minireview is intended to provide an explanatory overview of some related research, with the hope to invite innovations from areas with burgeoning new techniques.

Indexed as

C─S bond activationC─S bond metathesismetathesis reactionsingle‐bond metathesissynthesis of sulfides

Identifiers

PMID42631568
PMCPMC13499425

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.