Evidence map›Paper›PMID 38699278›Full record

ArticleChemical science2024

Visible-light-enabled stereoselective synthesis of functionalized cyclohexylamine derivatives

Yi-Nan Lu, Chao Che, Guangjin Zhen, Xin Chang, Xiu-Qin Dong, Chun-Jiang Wang

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. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Yi-Nan LuCollege of Chemistry and Molecular Sciences, Engineering Research Center of Organosilicon Compounds & Materials, Ministry of Education, Wuhan University Wuhan Hubei 430072 China xiuqindong@whu.edu.cn cjwang@whu.edu.cn.
Chao CheCollege of Chemistry and Molecular Sciences, Engineering Research Center of Organosilicon Compounds & Materials, Ministry of Education, Wuhan University Wuhan Hubei 430072 China xiuqindong@whu.edu.cn cjwang@whu.edu.cn.ORCID https://orcid.org/0000-0003-4643-1722
Guangjin ZhenCollege of Chemistry and Molecular Sciences, Engineering Research Center of Organosilicon Compounds & Materials, Ministry of Education, Wuhan University Wuhan Hubei 430072 China xiuqindong@whu.edu.cn cjwang@whu.edu.cn.
Xin ChangCollege of Chemistry and Molecular Sciences, Engineering Research Center of Organosilicon Compounds & Materials, Ministry of Education, Wuhan University Wuhan Hubei 430072 China xiuqindong@whu.edu.cn cjwang@whu.edu.cn.
Xiu-Qin DongCollege of Chemistry and Molecular Sciences, Engineering Research Center of Organosilicon Compounds & Materials, Ministry of Education, Wuhan University Wuhan Hubei 430072 China xiuqindong@whu.edu.cn cjwang@whu.edu.cn.ORCID https://orcid.org/0000-0002-5045-1198
Chun-Jiang WangCollege of Chemistry and Molecular Sciences, Engineering Research Center of Organosilicon Compounds & Materials, Ministry of Education, Wuhan University Wuhan Hubei 430072 China xiuqindong@whu.edu.cn cjwang@whu.edu.cn.ORCID https://orcid.org/0000-0003-3629-6889

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An unprecedented intermolecular [4 + 2] cycloaddition of benzocyclobutylamines with α-substituted vinylketones, enabled by photoredox catalysis, has been developed. The current method enables facile access to highly functionalized cyclohexylamine derivatives that were otherwise inaccessible, in moderate to good yields with excellent diastereoselectivities. This protocol has some excellent features, such as full atom economy, good functional-group compatibility, mild reaction conditions, and an overall redox-neutral process. Additionally, an asymmetric version of this cycloaddition was preliminarily investigated

Identifiers

PMID38699278
PMCPMC11062095

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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.