Evidence map›Paper›PMID 34168777›Full record

ArticleChemical science2021

Nickel-catalyzed asymmetric reductive arylation of α-chlorosulfones with aryl halides.

Deli Sun, Guobin Ma, Xinluo Zhao, Chuanhu Lei, Hegui Gong

Abstract read
In one paragraph

Article in Chemical science, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

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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.

Deli SunCenter for Supramolecular Chemistry and Catalysis, College of Sciences, Shanghai University 99 Shang-Da Road Shanghai 200444 China hegui_gong@shu.edu.cn chlei@shu.edu.cn.ORCID https://orcid.org/0000-0003-3098-3717
Guobin MaCenter for Supramolecular Chemistry and Catalysis, College of Sciences, Shanghai University 99 Shang-Da Road Shanghai 200444 China hegui_gong@shu.edu.cn chlei@shu.edu.cn.ORCID https://orcid.org/0000-0002-6291-8875
Xinluo ZhaoCenter for Supramolecular Chemistry and Catalysis, College of Sciences, Shanghai University 99 Shang-Da Road Shanghai 200444 China hegui_gong@shu.edu.cn chlei@shu.edu.cn.ORCID https://orcid.org/0000-0003-2139-8583
Chuanhu LeiCenter for Supramolecular Chemistry and Catalysis, College of Sciences, Shanghai University 99 Shang-Da Road Shanghai 200444 China hegui_gong@shu.edu.cn chlei@shu.edu.cn.ORCID https://orcid.org/0000-0002-0276-1132
Hegui GongCenter for Supramolecular Chemistry and Catalysis, College of Sciences, Shanghai University 99 Shang-Da Road Shanghai 200444 China hegui_gong@shu.edu.cn chlei@shu.edu.cn.ORCID https://orcid.org/0000-0001-6534-5569

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report an asymmetric Ni-catalyzed reductive cross-coupling of aryl/heteroaryl halides with racemic α-chlorosulfones to afford enantioenriched sulfones. The reaction tolerates a variety of functional groups under mild reaction conditions, which complements the current methods. The utility of this work was demonstrated by facile late-stage functionalization of commercial drugs.

Identifiers

PMID34168777
PMCPMC8179603

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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.