Evidence map›Paper›PMID 37945832›Full record

ArticleNature chemistry2024

Discovery and synthesis of atropisomerically chiral acyl-substituted stable vinyl sulfoxonium ylides.

Fengjin Wu, Yichi Zhang, Ruiqi Zhu, Yong Huang

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In one paragraph

Article in Nature chemistry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Azapeptide Atropisomers From Late-StageThe Journal of organic chemistry · 2025
    Article
  6. Article
  7. 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

4 authors.

Fengjin WuThe Department of Chemistry, The Hong Kong University of Science and Technology, Hong Kong SAR, China.ORCID http://orcid.org/0000-0002-4602-0184
Yichi ZhangThe Department of Chemistry, The Hong Kong University of Science and Technology, Hong Kong SAR, China.
Ruiqi ZhuThe Department of Chemistry, The Hong Kong University of Science and Technology, Hong Kong SAR, China.ORCID http://orcid.org/0009-0009-9095-1080
Yong HuangThe Department of Chemistry, The Hong Kong University of Science and Technology, Hong Kong SAR, China. yonghuang@ust.hk.ORCID http://orcid.org/0000-0001-8377-8923

Funding

National Natural Science Foundation of China (National Science Foundation of China) 21825101Research Grants Council, University Grants Committee (RGC, UGC) 16300320Research Grants Council, University Grants Committee (RGC, UGC) 16302122Research Grants Council, University Grants Committee (RGC, UGC) 16309021
6 · The paper itself

Abstract

Atropisomerism is a type of conformational chirality that plays a critical role in various fields of chemistry, including synthetic, medicinal and material chemistry, and its impact has been widely recognized. Although chiral atropisomerism in rotationally restricted aryl-aryl bonds has garnered substantial interest and led to important discoveries in chiral catalysts and drug development, the exploration of non-aryl atropisomers has fallen behind. Here we reveal a previously unexplored form of non-aryl atropisomerism by linking a sterically congested olefin to a sulfoxonium ylide. A streamlined synthetic approach to these novel molecules was developed through the hydrofunctionalization of alkynyl sulfoxonium ylides. Notably, an enantioselective organocatalytic strategy was developed to prepare these non-aryl atropisomers in high optical purity. This form of atropisomerism offers new routes for investigating the functional properties of axially chiral molecules.

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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.