Evidence map›Paper›PMID 37886104›Full record

ArticleChemical science2023

Coordinating activation strategy enables 1,2-alkylamidation of alkynes.

Jing Ren, Junhua Xu, Xiangxiang Kong, Jinlong Li, Kaizhi Li

Abstract read
In one paragraph

Article in Chemical science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

5 authors.

Jing RenBiopharmaceutical Research Institute, West China Hospital of Sichuan University 37 Guoxue Alley Chengdu 610041 P. R. China kzli@scu.edu.cn.
Junhua XuBiopharmaceutical Research Institute, West China Hospital of Sichuan University 37 Guoxue Alley Chengdu 610041 P. R. China kzli@scu.edu.cn.
Xiangxiang KongBiopharmaceutical Research Institute, West China Hospital of Sichuan University 37 Guoxue Alley Chengdu 610041 P. R. China kzli@scu.edu.cn.
Jinlong LiBiopharmaceutical Research Institute, West China Hospital of Sichuan University 37 Guoxue Alley Chengdu 610041 P. R. China kzli@scu.edu.cn.
Kaizhi LiBiopharmaceutical Research Institute, West China Hospital of Sichuan University 37 Guoxue Alley Chengdu 610041 P. R. China kzli@scu.edu.cn.ORCID https://orcid.org/0000-0003-1358-620X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The radical 1,2-difunctionalization reaction of alkynes has been evolved into a versatile approach for expeditiously increasing the complexity of the common feedstock alkyne. However, intermolecular 1,2-carboamidation with general alkyl groups is an unsolved problem. Herein, we show that a coordinating activation strategy could act as an efficient tool for enabling radical 1,2-alkylamidation of alkynes. With the employment of diacyl peroxides as both alkylating reagents and internal oxidants, a large library of β-alkylated enamides is constructed in a three-component manner from readily accessible amides and alkynes. This protocol exhibits broad substrate scope with good functional group compatibility and is amenable for late-stage functionalization of natural molecules and biologically compounds.

Identifiers

PMID37886104
PMCPMC10599465

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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.