Evidence map›Paper›PMID 38675603›Full record

ArticleMolecules (Basel, Switzerland)2024

Photoinduced Site-Selective Aryl C-H Borylation with Electron-Donor-Acceptor Complex Derived from B

Manhong Li, Yi-Hui Deng, Qianqian Chang, Jinyuan Li, Chao Wang, Leifeng Wang, Tian-Yu Sun

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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

7 authors.

Manhong LiKey Lab of Computational Chemistry and Drug Design, State Key Laboratory of Chemical Oncogenomics, School of Chemical Biology and Biotechnology, Peking University Shenzhen Graduate School, Shenzhen 518055, China.
Yi-Hui DengKey Lab of Computational Chemistry and Drug Design, State Key Laboratory of Chemical Oncogenomics, School of Chemical Biology and Biotechnology, Peking University Shenzhen Graduate School, Shenzhen 518055, China.
Qianqian ChangSchool of Pharmaceutical Sciences (Shenzhen), Sun Yat-sen University, No. 66, Gongchang Road, Shenzhen 518107, China.ORCID 0000-0003-1056-7556
Jinyuan LiShanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Lingling Lu, Shanghai 200032, China.
Chao WangKey Lab of Computational Chemistry and Drug Design, State Key Laboratory of Chemical Oncogenomics, School of Chemical Biology and Biotechnology, Peking University Shenzhen Graduate School, Shenzhen 518055, China.
Leifeng WangSchool of Pharmaceutical Sciences (Shenzhen), Sun Yat-sen University, No. 66, Gongchang Road, Shenzhen 518107, China.
Tian-Yu SunKey Lab of Computational Chemistry and Drug Design, State Key Laboratory of Chemical Oncogenomics, School of Chemical Biology and Biotechnology, Peking University Shenzhen Graduate School, Shenzhen 518055, China.ORCID 0000-0002-7746-479X

Funding

Shenzhen Science and Technology Program RCBS20210706092258097the Fundamental Research Funds for the Central Universities 23ykbj010the Guangdong Basic and Applied Basic Research Foundation 2022A1515011994the National Natural Science Foundation of China 21933004the National Natural Science Foundation of China 22271316the Sun Yat-sen University Startup Fund startup fundthe Technology & Innovation Commission of Shenzhen Municipality SZBH202103
6 · The paper itself

Abstract

Due to boron's metalloid properties, aromatic boron reagents are prevalent synthetic intermediates. The direct borylation of aryl C-H bonds for producing aromatic boron compounds offers an appealing, one-step solution. Despite significant advances in this field, achieving regioselective aryl C-H bond borylation using simple and readily available starting materials still remains a challenge. In this work, we attempted to enhance the reactivity of the electron-donor-acceptor (EDA) complex by selecting different bases to replace the organic base (NEt

Indexed as

B2Pin2borylationC-H bondelectron-donor-acceptorisoquinolinephotocatalysis

Identifiers

PMID38675603
PMCPMC11052414

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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.