Evidence map›Paper›PMID 42660935›Full record

ArticleNature communications2026

Bis(trifluoromethylthio)carbene as a toolbox for versatile carbene transformations.

Jun Sun, Qin-Yuan Ni, Yu-Cheng Gu, Jin-Hong Lin, Ji-Chang Xiao

Abstract read
PubMed Full text at PMC Publisher
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

5 authors.

Jun SunState Key Laboratory of Fluorine and Nitrogen Chemistry and Advanced Materials, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Shanghai, China.
Qin-Yuan NiState Key Laboratory of Fluorine and Nitrogen Chemistry and Advanced Materials, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Shanghai, China.
Yu-Cheng GuSyngenta Jealott's Hill International Research Centre, Bracknell, UK.ORCID http://orcid.org/0000-0002-6400-6167
Jin-Hong LinState Key Laboratory of Fluorine and Nitrogen Chemistry and Advanced Materials, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Shanghai, China. jlin@shu.edu.cn.ORCID http://orcid.org/0000-0002-7000-9540
Ji-Chang XiaoState Key Laboratory of Fluorine and Nitrogen Chemistry and Advanced Materials, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Shanghai, China. jchxiao@sioc.ac.cn.ORCID http://orcid.org/0000-0001-8881-1796

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Carbenes are highly valued for their broad utility across diverse fields, and their chemistry has consequently been the subject of extensive research. Taming the high reactivity of these divalent carbon intermediates to achieve controllable selectivity for diverse transformations remains a fundamental challenge. This often necessitates bespoke, fine-tuned conditions for each reaction type, limiting generality and efficiency. Here, we report the rational design of a versatile, electrophilic carbene-bis(trifluoromethylthio)carbene (:C(SCF

Identifiers

PMID42660935
PMCPMC13522504

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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.