Evidence map›Paper›PMID 37655018›Full record

ArticleChemical science2023

Highly enantioselective synthesis of both tetrahydroquinoxalines and dihydroquinoxalinones

Ana Xu, Chaoyi Li, Junrong Huang, Heng Pang, Chengyao Zhao, Lijuan Song, Hengzhi You, Xumu Zhang, Fen-Er Chen

Open access · diamondAbstract read
PubMed Full text at PMC Publisher
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
1.6field-weighted citation impact, top 18% 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

1 citing paper in PubMed, 16 citations in OpenAlex.

  1. Review
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

9 authors at 2 institutions in 1 country.

Ana XuSchool of Science, Harbin Institute of Technology (Shenzhen) Taoyuan Street, Nanshan District Shenzhen 518055 China songlijuan@hit.edu.cn youhengzhi@hit.edu.cn rfchen@fudan.edu.cn.
Chaoyi LiSchool of Science, Harbin Institute of Technology (Shenzhen) Taoyuan Street, Nanshan District Shenzhen 518055 China songlijuan@hit.edu.cn youhengzhi@hit.edu.cn rfchen@fudan.edu.cn.ORCID https://orcid.org/0000-0002-2639-0516
Junrong HuangSchool of Science, Harbin Institute of Technology (Shenzhen) Taoyuan Street, Nanshan District Shenzhen 518055 China songlijuan@hit.edu.cn youhengzhi@hit.edu.cn rfchen@fudan.edu.cn.ORCID https://orcid.org/0000-0001-8647-5418
Heng PangSchool of Science, Harbin Institute of Technology (Shenzhen) Taoyuan Street, Nanshan District Shenzhen 518055 China songlijuan@hit.edu.cn youhengzhi@hit.edu.cn rfchen@fudan.edu.cn.
Chengyao ZhaoSchool of Science, Harbin Institute of Technology (Shenzhen) Taoyuan Street, Nanshan District Shenzhen 518055 China songlijuan@hit.edu.cn youhengzhi@hit.edu.cn rfchen@fudan.edu.cn.
Lijuan SongSchool of Science, Harbin Institute of Technology (Shenzhen) Taoyuan Street, Nanshan District Shenzhen 518055 China songlijuan@hit.edu.cn youhengzhi@hit.edu.cn rfchen@fudan.edu.cn.
Hengzhi YouSchool of Science, Harbin Institute of Technology (Shenzhen) Taoyuan Street, Nanshan District Shenzhen 518055 China songlijuan@hit.edu.cn youhengzhi@hit.edu.cn rfchen@fudan.edu.cn.ORCID https://orcid.org/0000-0001-8904-5050
Xumu ZhangDepartment of Chemistry, Shenzhen Grubbs Institute, Southern University of Science and Technology Shenzhen 518055 China.ORCID https://orcid.org/0000-0001-5700-0608
Fen-Er ChenSchool of Science, Harbin Institute of Technology (Shenzhen) Taoyuan Street, Nanshan District Shenzhen 518055 China songlijuan@hit.edu.cn youhengzhi@hit.edu.cn rfchen@fudan.edu.cn.ORCID https://orcid.org/0000-0002-6734-3388
Harbin Institute of Technology · CNSouthern University of Science and Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chiral tetrahydroquinoxalines and dihydroquinoxalinones represent the core structure of many bioactive molecules. Herein, a simple and efficient Rh-thiourea-catalyzed asymmetric hydrogenation for enantiopure tetrahydroquinoxalines and dihydroquinoxalinones was developed under 1 MPa H

Identifiers

PMID37655018
PMCPMC10466277
OpenAlexW4383424748

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.