Evidence map›Paper›PMID 35498572›Full record

ArticleRSC advances2020

Three-component reaction of azulene, aryl glyoxal and 1,3-dicarbonyl compound for the synthesis of various azulene derivatives.

Jing Gong, Anatoly A Peshkov, Jiafeng Yu, Sagadat Amandykova, Aidana Gimnkhan, Jianjun Huang, Stepan Kashtanov, Olga P Pereshivko, Vsevolod A Peshkov

Open access · goldAbstract read
In one paragraph

Article in RSC advances, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 35% 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

2 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. 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

9 authors at 3 institutions in 2 countries.

Jing GongCollege of Chemistry, Chemical Engineering and Materials Science, Soochow University Dushu Lake Campus Suzhou 215123 P. R. China olga@suda.edu.cn vsevolod@suda.edu.cn.
Anatoly A PeshkovDepartment of Chemistry, School of Sciences and Humanities, Nazarbayev University 53 Kabanbay Batyr Ave, Block 7 Nur-Sultan 010000 Republic of Kazakhstan, olga.pereshivko@nu.edu.kz vsevolod.peshkov@nu.edu.kz.
Jiafeng YuCollege of Chemistry, Chemical Engineering and Materials Science, Soochow University Dushu Lake Campus Suzhou 215123 P. R. China olga@suda.edu.cn vsevolod@suda.edu.cn.
Sagadat AmandykovaDepartment of Chemistry, School of Sciences and Humanities, Nazarbayev University 53 Kabanbay Batyr Ave, Block 7 Nur-Sultan 010000 Republic of Kazakhstan, olga.pereshivko@nu.edu.kz vsevolod.peshkov@nu.edu.kz.
Aidana GimnkhanDepartment of Chemistry, School of Sciences and Humanities, Nazarbayev University 53 Kabanbay Batyr Ave, Block 7 Nur-Sultan 010000 Republic of Kazakhstan, olga.pereshivko@nu.edu.kz vsevolod.peshkov@nu.edu.kz.
Jianjun HuangCollege of Chemistry, Chemical Engineering and Materials Science, Soochow University Dushu Lake Campus Suzhou 215123 P. R. China olga@suda.edu.cn vsevolod@suda.edu.cn.
Stepan KashtanovDepartment of Chemistry, Xi'an Jiaotong-Liverpool University Suzhou 215123 P. R. China.
Olga P PereshivkoCollege of Chemistry, Chemical Engineering and Materials Science, Soochow University Dushu Lake Campus Suzhou 215123 P. R. China olga@suda.edu.cn vsevolod@suda.edu.cn.
Vsevolod A PeshkovCollege of Chemistry, Chemical Engineering and Materials Science, Soochow University Dushu Lake Campus Suzhou 215123 P. R. China olga@suda.edu.cn vsevolod@suda.edu.cn.ORCID https://orcid.org/0000-0001-6649-2384
Soochow University · CNNazarbayev University · KZXi’an Jiaotong-Liverpool University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A three-component reaction of an azulene, an aryl glyoxal and a 1,3-dicarbonyl compound has been elaborated to access a series of azulene derivatives. Some of these azulene-containing adducts were further subjected to post-MCR transformations to assemble azulene-heterocycle conjugates.

Identifiers

PMID35498572
PMCPMC9050217
OpenAlexW3012380301

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.