Evidence map›Paper›PMID 31252657›Full record

ArticleMolecules (Basel, Switzerland)2019

Synthesis and Properties of 6-Aryl-4-azidocinnolines and 6-Aryl-4-(1,2,3-1

Natalia A Danilkina, Nina S Bukhtiiarova, Anastasia I Govdi, Anna A Vasileva, Andrey M Rumyantsev, Artemii A Volkov, Nikita I Sharaev, Alexey V Povolotskiy, Irina A Boyarskaya, Ilya V Kornyakov and 2 more

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Modern Strategies for Heterocycle Synthesis.Molecules (Basel, Switzerland) · 2020
    Article
  5. 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

12 authors.

Natalia A DanilkinaInstitute of Chemistry, Saint Petersburg State University (SPSU), Universitetskaya nab. 7/9, Saint Petersburg 199034, Russia.ORCID 0000-0002-1693-0056
Nina S BukhtiiarovaInstitute of Chemistry, Saint Petersburg State University (SPSU), Universitetskaya nab. 7/9, Saint Petersburg 199034, Russia.
Anastasia I GovdiInstitute of Chemistry, Saint Petersburg State University (SPSU), Universitetskaya nab. 7/9, Saint Petersburg 199034, Russia.
Anna A VasilevaInstitute of Chemistry, Saint Petersburg State University (SPSU), Universitetskaya nab. 7/9, Saint Petersburg 199034, Russia.
Andrey M RumyantsevDepartment of Genetics and Biotechnology, Saint Petersburg State University (SPSU), Universitetskaya nab. 7/9, Saint Petersburg 199034, Russia.
Artemii A VolkovDepartment of Genetics and Biotechnology, Saint Petersburg State University (SPSU), Universitetskaya nab. 7/9, Saint Petersburg 199034, Russia.ORCID 0000-0002-9375-2943
Nikita I SharaevDepartment of Genetics and Biotechnology, Saint Petersburg State University (SPSU), Universitetskaya nab. 7/9, Saint Petersburg 199034, Russia.
Alexey V PovolotskiyInstitute of Chemistry, Saint Petersburg State University (SPSU), Universitetskaya nab. 7/9, Saint Petersburg 199034, Russia.ORCID 0000-0001-7931-9572
Irina A BoyarskayaInstitute of Chemistry, Saint Petersburg State University (SPSU), Universitetskaya nab. 7/9, Saint Petersburg 199034, Russia.
Ilya V KornyakovInstitute of Chemistry, Saint Petersburg State University (SPSU), Universitetskaya nab. 7/9, Saint Petersburg 199034, Russia.ORCID 0000-0002-8904-6149
Polina V TokarevaInstitute of Chemistry, Saint Petersburg State University (SPSU), Universitetskaya nab. 7/9, Saint Petersburg 199034, Russia.
Irina A BalovaInstitute of Chemistry, Saint Petersburg State University (SPSU), Universitetskaya nab. 7/9, Saint Petersburg 199034, Russia. i.balova@spbu.ru.ORCID 0000-0002-8593-4755

Funding

Russian Foundation for Basic Research 18-33-01265
6 · The paper itself

Abstract

An efficient approach towards the synthesis of 6-aryl-4-azidocinnolines was developed with the aim of exploring the photophysical properties of 6-aryl-4-azidocinnolines and their click reaction products with alkynes, 6-aryl-4-(1,2,3-1

Indexed as

Antineoplastic AgentsCell SurvivalClick ChemistryHeLa CellsHeterocyclic Compounds, 2-RingHumansMolecular StructureTriazolesAntineoplastic AgentsHeterocyclic Compounds, 2-RingTriazolesalkynesazidescinnolinesCuAACcycloalkynescytotoxicityfluorescenceRichter cyclizationSuzuki couplingtriazoles

Identifiers

PMID31252657
PMCPMC6651781

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.