Evidence map›Paper›PMID 34163805›Full record

ArticleChemical science2020

Understanding the unique reactivity patterns of nickel/JoSPOphos manifold in the nickel-catalyzed enantioselective C-H cyclization of imidazoles.

Jian-Biao Liu, Xin Wang, Antonis M Messinis, Xiao-Jun Liu, Rositha Kuniyil, De-Zhan Chen, Lutz Ackermann

Open access · diamondAbstract read
In one paragraph

Article in Chemical science, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
2.0field-weighted citation impact, top 14% of its field
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

1 citing paper in PubMed, 23 citations in OpenAlex.

  1. Article
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

7 authors at 2 institutions in 2 countries.

Jian-Biao LiuCollege of Chemistry, Chemical Engineering and Materials Science, Shandong Normal University Jinan 250014 China jianbiaoliu.thu@gmail.com chendzh@sdnu.edu.cn.ORCID https://orcid.org/0000-0002-2550-3355
Xin WangCollege of Chemistry, Chemical Engineering and Materials Science, Shandong Normal University Jinan 250014 China jianbiaoliu.thu@gmail.com chendzh@sdnu.edu.cn.
Antonis M MessinisInstitut für Organische und Biomolekulare Chemie, Georg-August-Universität Göttingen Göttingen 37077 Germany Lutz.Ackermann@chemie.uni-goettingen.de.ORCID https://orcid.org/0000-0002-6168-355X
Xiao-Jun LiuCollege of Chemistry, Chemical Engineering and Materials Science, Shandong Normal University Jinan 250014 China jianbiaoliu.thu@gmail.com chendzh@sdnu.edu.cn.ORCID https://orcid.org/0000-0002-5624-5109
Rositha KuniyilInstitut für Organische und Biomolekulare Chemie, Georg-August-Universität Göttingen Göttingen 37077 Germany Lutz.Ackermann@chemie.uni-goettingen.de.
De-Zhan ChenCollege of Chemistry, Chemical Engineering and Materials Science, Shandong Normal University Jinan 250014 China jianbiaoliu.thu@gmail.com chendzh@sdnu.edu.cn.ORCID https://orcid.org/0000-0002-2192-4582
Lutz AckermannInstitut für Organische und Biomolekulare Chemie, Georg-August-Universität Göttingen Göttingen 37077 Germany Lutz.Ackermann@chemie.uni-goettingen.de.ORCID https://orcid.org/0000-0001-7034-8772
Shandong Normal University · CNUniversity of Göttingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The 3d transition metal-catalyzed enantioselective C-H functionalization provides a sustainable strategy for the construction of chiral molecules. A better understanding of the catalytic nature of the reactions and the factors controlling the enantioselectivity is important for rational design of more efficient systems. Herein, the mechanisms of Ni-catalyzed enantioselective C-H cyclization of imidazoles are investigated by density functional theory (DFT) calculations. Both the π-allyl nickel(ii)-promoted σ-complex-assisted metathesis (σ-CAM) and the nickel(0)-catalyzed oxidative addition (OA) mechanisms are disfavored. In addition to the typically proposed ligand-to-ligand hydrogen transfer (LLHT) mechanism, the reaction can also proceed

Identifiers

PMID34163805
PMCPMC8178989
OpenAlexW3097970532

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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.