Evidence map›Paper›PMID 37660185›Full record

ArticleNature communications2023

Organophotocatalysed synthesis of 2-piperidinones in one step via [1 + 2 + 3] strategy.

Yi-Dan Du, Shan Wang, Hai-Wu Du, Xiao-Yong Chang, Xiao-Yi Chen, Yu-Long Li, Wei Shu

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 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
4.0field-weighted citation impact, top 5% 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

7 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
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  3. Article
  4. Article
  5. Review
  6. Design and Preparation of Heterostructured CuMolecules (Basel, Switzerland) · 2024
    Review
  7. Dialkylation of CFNature communications · 2024
    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

7 authors at 3 institutions in 1 country.

Yi-Dan Du *Shenzhen Grubbs Institute and Department of Chemistry, Southern University of Science and Technology, Shenzhen, 518055, Guangdong, P. R. China.
Shan Wang *Shenzhen Grubbs Institute and Department of Chemistry, Southern University of Science and Technology, Shenzhen, 518055, Guangdong, P. R. China.
Hai-Wu DuShenzhen Grubbs Institute and Department of Chemistry, Southern University of Science and Technology, Shenzhen, 518055, Guangdong, P. R. China.
Xiao-Yong ChangShenzhen Grubbs Institute and Department of Chemistry, Southern University of Science and Technology, Shenzhen, 518055, Guangdong, P. R. China.ORCID http://orcid.org/0000-0003-1394-6164
Xiao-Yi ChenShenzhen Grubbs Institute and Department of Chemistry, Southern University of Science and Technology, Shenzhen, 518055, Guangdong, P. R. China.
Yu-Long LiCollege of Chemistry and Environmental Engineering, Sichuan University of Science and Engineering, 643000, Zigong, P. R. China.
Wei ShuShenzhen Grubbs Institute and Department of Chemistry, Southern University of Science and Technology, Shenzhen, 518055, Guangdong, P. R. China. shuw@sustech.edu.cn.ORCID http://orcid.org/0000-0003-0890-2634
Southern University of Science and Technology · CNNankai University · CNSichuan University of Science and Engineering · CN

Funding

Department of Education of Guangdong Province (Guangdong Province Education Department) 2022JGXM054, 2021KTSCX106Guangdong Science and Technology Department (Science and Technology Department, Guangdong Province) 2019QN01Y261, 2020B121201002National Science Foundation of China | Major Research Plan 21971101, 22171127, 22371129Natural Science Foundation of Guangdong Province (Guangdong Natural Science Foundation) 2022A1515011806Shenzhen Science and Technology Innovation Commission JCYJ20220519201425001
6 · The paper itself

Abstract

Six-membered N-containing heterocycles, such as 2-piperidinone derivatives, with diverse substitution patterns are widespread in natural products, drug molecules and serve as key precursors for piperidines. Thus, the development of stereoselective synthesis of multi-substituted 2-piperidinones are attractive. However, existing methods heavily rely on modification of pre-synthesized backbones which require tedious multi-step procedure and suffer from limited substitution patterns. Herein, an organophotocatalysed [1 + 2 + 3] strategy was developed to enable the one-step access to diverse substituted 2-piperidinones from easily available inorganic ammonium salts, alkenes, and unsaturated carbonyl compounds. This mild protocol exhibits exclusive chemoselectivity over two alkenes, tolerating both terminal and internal alkenes with a wide range of functional groups.

Identifiers

PMID37660185
PMCPMC10475035
OpenAlexW4386392768

What OpenQuestion holds

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LicenceCC BY
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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.