Desulfonylative Functionalization of Organosulfones via Inert (Hetero)Aryl C(

Rui Huang, Boning Gu, Ming Wang, Yinsong Zhao, Xuefeng Jiang

Abstract readReview

In one paragraph

Review in Molecules (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it

0cells of the map it votes in

2citing 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

2 citing papers in PubMed.

Development of a multi-targeted sulfonyl-bridged bisselenadiazole derivative as a potent EGFR/PI3K/AKT/mTOR modulator in lung adenocarcinoma.RSC advances · 2026
Article
Recent Advances in C-C Bond Formation via Visible Light-Mediated Desulfonylation and Its Application in the Modification of Biologically Active Compounds.Molecules (Basel, Switzerland) · 2024
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

5 authors.

Rui HuangState Key Laboratory of Estuarine and Coastal Research, Hainan Institute of East China Normal University, East China Normal University, Shanghai 200241, China.

Boning GuState Key Laboratory of Petroleum Molecular & Process Engineering, Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering, East China Normal University, Shanghai 200062, China.

Ming WangState Key Laboratory of Petroleum Molecular & Process Engineering, Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering, East China Normal University, Shanghai 200062, China.

Yinsong ZhaoState Key Laboratory of Estuarine and Coastal Research, Hainan Institute of East China Normal University, East China Normal University, Shanghai 200241, China.ORCID 0000-0002-2480-0294

Xuefeng JiangState Key Laboratory of Estuarine and Coastal Research, Hainan Institute of East China Normal University, East China Normal University, Shanghai 200241, China.

Funding

National Natural Science Foundation of China 22125103 and 22301077Shanghai Pujiang Program 22PJ1403200

6 · The paper itself

Abstract

As "chemical chameleons," organosulfones have been widely applied in various desulfonylative functionalization reactions. However, the desulfonylative functionalization of (hetero)arylsulfones through the cleavage of inert C(

Indexed as

C(sp2)–SO2 bond cleavagedesulfonylative functionalization(hetero)arylsulfonesphotocatalysistransition-metal catalysis

Identifiers

PMID39274985

DOI10.3390/molecules29174137

PMCPMC11397149

What OpenQuestion holds

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Registered trials

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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.