Evidence map›Paper›PMID 39183900›Full record

ArticleChemical science2024

Enantioconvergent and diastereoselective synthesis of atropisomeric hydrazides bearing a cyclic quaternary stereocenter through ternary catalysis.

Xia Wang, Shao-Jie Wang, Xiaolan Xin, Hao An, Zhifeng Tu, Hui Yang, Ming Wah Wong, Shenci Lu

Abstract read
In one paragraph

Article in Chemical science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Azapeptide Atropisomers From Late-StageThe Journal of organic chemistry · 2025
    Article
  2. 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

8 authors.

Xia WangFrontiers Science Center for Flexible Electronics (FSCFE), Shaanxi Institute of Flexible Electronics (SIFE), Shaanxi Institute of Biomedical Materials and Engineering (SIBME), Northwestern Polytechnical University (NPU) 127 West Youyi Road Xi'an 710072 China iamzftu@nwpu.edu.cn iamsclu@nwpu.edu.cn.
Shao-Jie WangFrontiers Science Center for Flexible Electronics (FSCFE), Shaanxi Institute of Flexible Electronics (SIFE), Shaanxi Institute of Biomedical Materials and Engineering (SIBME), Northwestern Polytechnical University (NPU) 127 West Youyi Road Xi'an 710072 China iamzftu@nwpu.edu.cn iamsclu@nwpu.edu.cn.
Xiaolan XinFrontiers Science Center for Flexible Electronics (FSCFE), Shaanxi Institute of Flexible Electronics (SIFE), Shaanxi Institute of Biomedical Materials and Engineering (SIBME), Northwestern Polytechnical University (NPU) 127 West Youyi Road Xi'an 710072 China iamzftu@nwpu.edu.cn iamsclu@nwpu.edu.cn.
Hao AnFrontiers Science Center for Flexible Electronics (FSCFE), Shaanxi Institute of Flexible Electronics (SIFE), Shaanxi Institute of Biomedical Materials and Engineering (SIBME), Northwestern Polytechnical University (NPU) 127 West Youyi Road Xi'an 710072 China iamzftu@nwpu.edu.cn iamsclu@nwpu.edu.cn.
Zhifeng TuFrontiers Science Center for Flexible Electronics (FSCFE), Shaanxi Institute of Flexible Electronics (SIFE), Shaanxi Institute of Biomedical Materials and Engineering (SIBME), Northwestern Polytechnical University (NPU) 127 West Youyi Road Xi'an 710072 China iamzftu@nwpu.edu.cn iamsclu@nwpu.edu.cn.
Hui YangDepartment of Chemistry, National University of Singapore 3 Science Drive 3 Singapore 117543 Singapore chmwmw@nus.edu.sg.ORCID https://orcid.org/0000-0002-0435-6763
Ming Wah WongDepartment of Chemistry, National University of Singapore 3 Science Drive 3 Singapore 117543 Singapore chmwmw@nus.edu.sg.ORCID https://orcid.org/0000-0003-2162-1220
Shenci LuFrontiers Science Center for Flexible Electronics (FSCFE), Shaanxi Institute of Flexible Electronics (SIFE), Shaanxi Institute of Biomedical Materials and Engineering (SIBME), Northwestern Polytechnical University (NPU) 127 West Youyi Road Xi'an 710072 China iamzftu@nwpu.edu.cn iamsclu@nwpu.edu.cn.ORCID https://orcid.org/0000-0003-4357-455X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An efficient and highly enantioconvergent and diastereoselective ternary catalysis in a one-pot process is reported, which represents an integrated strategy for the synthesis of atropisomeric hydrazides with defined vicinal central and axial chirality from readily available racemic α-amino-ynones, azodicarboxylates, and Morita-Baylis-Hillman (MBH) carbonates. This method utilizes

Identifiers

PMID39183900
PMCPMC11339960

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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.