Evidence map›Paper›PMID 34377393›Full record

ArticleChemical science2021

Catalytic asymmetric synthesis of spirocyclobutyl oxindoles and beyond

Xia Zhong, Jiuqi Tan, Jianglin Qiao, Yuqiao Zhou, Cidan Lv, Zhishan Su, Shunxi Dong, Xiaoming Feng

Open access · diamondAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Chemical science, 2021. 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
2.7field-weighted citation impact, top 9% 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

0 citing papers in PubMed, 37 citations in OpenAlex.

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

8 authors at 1 institution in 2 countries.

Xia ZhongKey Laboratory of Green Chemistry & Technology, Ministry of Education, College of Chemistry, Sichuan University Chengdu 610064 China dongs@scu.edu.cn xmfeng@scu.edu.cn http://www.scu.edu.cn/chem_asl/.ORCID https://orcid.org/0000-0003-4934-7040
Jiuqi TanKey Laboratory of Green Chemistry & Technology, Ministry of Education, College of Chemistry, Sichuan University Chengdu 610064 China dongs@scu.edu.cn xmfeng@scu.edu.cn http://www.scu.edu.cn/chem_asl/.
Jianglin QiaoKey Laboratory of Green Chemistry & Technology, Ministry of Education, College of Chemistry, Sichuan University Chengdu 610064 China dongs@scu.edu.cn xmfeng@scu.edu.cn http://www.scu.edu.cn/chem_asl/.
Yuqiao ZhouKey Laboratory of Green Chemistry & Technology, Ministry of Education, College of Chemistry, Sichuan University Chengdu 610064 China dongs@scu.edu.cn xmfeng@scu.edu.cn http://www.scu.edu.cn/chem_asl/.ORCID https://orcid.org/0000-0003-3490-4182
Cidan LvKey Laboratory of Green Chemistry & Technology, Ministry of Education, College of Chemistry, Sichuan University Chengdu 610064 China dongs@scu.edu.cn xmfeng@scu.edu.cn http://www.scu.edu.cn/chem_asl/.
Zhishan SuKey Laboratory of Green Chemistry & Technology, Ministry of Education, College of Chemistry, Sichuan University Chengdu 610064 China dongs@scu.edu.cn xmfeng@scu.edu.cn http://www.scu.edu.cn/chem_asl/.ORCID https://orcid.org/0000-0001-5168-3823
Shunxi DongKey Laboratory of Green Chemistry & Technology, Ministry of Education, College of Chemistry, Sichuan University Chengdu 610064 China dongs@scu.edu.cn xmfeng@scu.edu.cn http://www.scu.edu.cn/chem_asl/.ORCID https://orcid.org/0000-0002-3018-3085
Xiaoming FengKey Laboratory of Green Chemistry & Technology, Ministry of Education, College of Chemistry, Sichuan University Chengdu 610064 China dongs@scu.edu.cn xmfeng@scu.edu.cn http://www.scu.edu.cn/chem_asl/.ORCID https://orcid.org/0000-0003-4507-0478
Sichuan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Efficient asymmetric synthesis of a collection of small molecules with structural diversity is highly important to drug discovery. Herein, three distinct types of chiral cyclic compounds were accessible by enantioselective catalysis and sequential transformations. Highly regio- and enantioselective [2+2] cycloaddition of (

Identifiers

PMID34377393
PMCPMC8317662
OpenAlexW3175930420

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.