Evidence map›Paper›PMID 36732532›Full record

ArticleNature communications2023

Achiral organoiodine-functionalized helical polyisocyanides for multiple asymmetric dearomative oxidations.

Zong-Quan Wu, Xue Song, Yan-Xiang Li, Li Zhou, Yuan-Yuan Zhu, Zheng Chen, Na Liu

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. 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
6.6field-weighted citation impact, top 2% 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

9 citing papers in PubMed, 44 citations in OpenAlex.

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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

7 authors at 2 institutions in 1 country.

Zong-Quan WuState Key Laboratory of Supramolecular Structureand Materials, College of Chemistry, Jilin University, Changchun, 130012, China. zqwu@jlu.edu.cn.ORCID http://orcid.org/0000-0001-6657-9316
Xue SongDepartment of Polymer Science and Engineering, School of Chemistry and Chemical Engineering, Hefei University of Technology, Hefei, 230009, China.
Yan-Xiang LiDepartment of Polymer Science and Engineering, School of Chemistry and Chemical Engineering, Hefei University of Technology, Hefei, 230009, China.
Li ZhouDepartment of Polymer Science and Engineering, School of Chemistry and Chemical Engineering, Hefei University of Technology, Hefei, 230009, China.
Yuan-Yuan ZhuDepartment of Polymer Science and Engineering, School of Chemistry and Chemical Engineering, Hefei University of Technology, Hefei, 230009, China.
Zheng ChenState Key Laboratory of Supramolecular Structureand Materials, College of Chemistry, Jilin University, Changchun, 130012, China.ORCID http://orcid.org/0000-0002-5567-522X
Na LiuThe School of Pharmaceutical Sciences, Jilin University, 1266 Fujin Road, Changchun, Jilin, 130021, China.
Hefei University of Technology · CNJilin University · CN

Funding

National Natural Science Foundation of China (National Science Foundation of China) 21871073National Natural Science Foundation of China (National Science Foundation of China) 21971052National Natural Science Foundation of China (National Science Foundation of China) 22071041National Natural Science Foundation of China (National Science Foundation of China) 51903072National Natural Science Foundation of China (National Science Foundation of China) 52273006National Natural Science Foundation of China (National Science Foundation of China) 52273204National Natural Science Foundation of China (National Science Foundation of China) 92256201
6 · The paper itself

Abstract

Immobilizing organocatalyst onto helical polymers not only facilitates the catalyst recycling from homogeneous reactions, but also boosts enantioselectivity. In this work, achiral organoiodine-functionalized single left- and right-handed helical polyisocyanides were prepared from the same monomers, which catalyzed three asymmetric oxidations gave the desired products in high yields and excellent enantioselectivity. The enantiomeric excess of the target products was up to 95%. Remarkably, the enantioselectivity can be switched by reversing the helicity of the polymer backbone. The polymer catalysts can be facilely recovered and recycled in different asymmetric oxidations with maintained excellent activity and enantioselectivity.

Identifiers

PMID36732532
PMCPMC9894859
OpenAlexW4318983430

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.