Evidence map›Paper›PMID 34349912›Full record

ArticleChemical science2021

Atroposelective synthesis of

Yong-Jie Wu, Pei-Pei Xie, Gang Zhou, Qi-Jun Yao, Xin Hong, Bing-Feng Shi

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 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Review
  3. Azapeptide Atropisomers From Late-StageThe Journal of organic chemistry · 2025
    Article
  4. Atroposelective catalysis.Nature reviews. Chemistry · 2024
    Review
  5. Article
  6. Review
  7. Asymmetric Synthesis of Axially Chiral C-N Atropisomers.Chemistry (Weinheim an der Bergstrasse, Germany) · 2022
    Review
  8. Article
  9. Article
  10. 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

6 authors.

Yong-Jie WuCenter of Chemistry for Frontier Technologies, Department of Chemistry, Zhejiang University Hangzhou 310027 China 3110000156@zju.edu.cn hxchem@zju.edu.cn bfshi@zju.edu.cn.
Pei-Pei XieCenter of Chemistry for Frontier Technologies, Department of Chemistry, Zhejiang University Hangzhou 310027 China 3110000156@zju.edu.cn hxchem@zju.edu.cn bfshi@zju.edu.cn.
Gang ZhouCenter of Chemistry for Frontier Technologies, Department of Chemistry, Zhejiang University Hangzhou 310027 China 3110000156@zju.edu.cn hxchem@zju.edu.cn bfshi@zju.edu.cn.
Qi-Jun YaoCenter of Chemistry for Frontier Technologies, Department of Chemistry, Zhejiang University Hangzhou 310027 China 3110000156@zju.edu.cn hxchem@zju.edu.cn bfshi@zju.edu.cn.
Xin HongCenter of Chemistry for Frontier Technologies, Department of Chemistry, Zhejiang University Hangzhou 310027 China 3110000156@zju.edu.cn hxchem@zju.edu.cn bfshi@zju.edu.cn.ORCID https://orcid.org/0000-0003-4717-2814
Bing-Feng ShiCenter of Chemistry for Frontier Technologies, Department of Chemistry, Zhejiang University Hangzhou 310027 China 3110000156@zju.edu.cn hxchem@zju.edu.cn bfshi@zju.edu.cn.ORCID https://orcid.org/0000-0003-0375-955X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The introduction of chirality into peptoids is an important strategy to determine a discrete and robust secondary structure. However, the lack of an efficient strategy for the synthesis of structurally diverse chiral peptoids has hampered the studies. Herein, we report the efficient synthesis of a wide variety of

Identifiers

PMID34349912
PMCPMC8278962

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.