Evidence map›Paper›PMID 39242562›Full record

ArticleNature communications2024

Simultaneous construction of inherent and axial chirality by cobalt-catalyzed enantioselective C-H activation of calix[4]arenes.

Tong Li, Yanbo Zhang, Cong Du, Dandan Yang, Mao-Ping Song, Jun-Long Niu

Abstract read
In one paragraph

Article in Nature communications, 2024. 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. Cobalt-Catalyzed Asymmetric Construction of Boron Stereocenters With C-N Axial Chirality.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  3. Organocatalytic Enantioselective Divergent Synthesis of Pillar[5]Arenes.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  4. Chemical science · 2026
    Article
  5. Installing Axial Chirality by Atroposelective C(spJournal of the American Chemical Society · 2026
    Article
  6. Article
  7. Article
  8. Review
  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.

Tong LiCollege of Chemistry, Pingyuan Laboratory, Zhengzhou University, Zhengzhou, China.
Yanbo ZhangCollege of Chemistry, Pingyuan Laboratory, Zhengzhou University, Zhengzhou, China.
Cong DuSchool of Materials Science and Engineering, and Collaborative Innovation Center of Nano Functional Materials and Applications, Henan University, Kaifeng, China.
Dandan YangCollege of Chemistry, Pingyuan Laboratory, Zhengzhou University, Zhengzhou, China. yangdandan@zzu.edu.cn.ORCID http://orcid.org/0000-0002-1880-8417
Mao-Ping SongCollege of Chemistry, Pingyuan Laboratory, Zhengzhou University, Zhengzhou, China.
Jun-Long NiuCollege of Chemistry, Pingyuan Laboratory, Zhengzhou University, Zhengzhou, China. niujunlong@zzu.edu.cn.ORCID http://orcid.org/0000-0001-8012-4676

Funding

National Natural Science Foundation of China (National Science Foundation of China) 22271260
6 · The paper itself

Abstract

The simultaneous construction of multiple stereogenic elements in a single step is highly appealing and desirable in the field of asymmetric synthesis. Furthermore, the catalytic enantioselective synthesis of inherently chiral calix[n]arenes with high enantiopurity has long been a challenging endeavor. Herein, we report an enantioselective cobalt-catalyzed C-H activation/annulation for the efficient construction of inherently chiral calix[4]arenes bearing multiple C-N axially chiral element. By employing the benzamide tethered calix[4]arene as the substrate, the C-H annulation with alkynes can be successfully accomplished, leading to the generation of multiple stereogenic elements. A wide range of calix[4]arenes and alkynes are found to be well compatible, and exhibit good yields, high enantioselectivity and excellent diastereoselectivity. Notably, the gram-scale reaction, catalytic application, synthetic transformations, and chiral recognition further showcase the potential applications of this protocol.

Identifiers

PMID39242562
PMCPMC11379863

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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.