SnAr Reactions of 2,4-Diazidopyrido[3,2-

Kristaps Leškovskis, Anatoly Mishnev, Irina Novosjolova, Māris Turks

Open access · goldAbstract read

In one paragraph

Article in Molecules (Basel, Switzerland), 2022. 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

0.4field-weighted citation impact, top 44% 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, 4 citations in OpenAlex.

SnAr Reactions of 2,4-Diazidopyrido[3,2-Molecules (Basel, Switzerland) · 2022
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

4 authors at 2 institutions in 1 country.

Kristaps LeškovskisInstitute of Technology of Organic Chemistry, Faculty of Materials Science and Applied Chemistry, Riga Technical University, P. Valdena str. 3, LV-1048 Riga, Latvia.

Anatoly MishnevLatvian Institute of Organic Synthesis, Aizkraukles str. 21, LV-1006 Riga, Latvia.

Irina NovosjolovaInstitute of Technology of Organic Chemistry, Faculty of Materials Science and Applied Chemistry, Riga Technical University, P. Valdena str. 3, LV-1048 Riga, Latvia.ORCID 0000-0002-9607-2222

Māris TurksInstitute of Technology of Organic Chemistry, Faculty of Materials Science and Applied Chemistry, Riga Technical University, P. Valdena str. 3, LV-1048 Riga, Latvia.ORCID 0000-0001-5227-0369

Riga Technical University · LVLatvijas Organiskās Sintēzes Institūts · LV

Funding

Central Finance and Contracting Agency of the Republic of Latvia European Social Fund within the Project No 8.2.2.0/20/I/008Latvian Council of Science LZP-2020/1-0348

6 · The paper itself

Abstract

A straightforward method for the synthesis of 5-substituted tetrazolo[1,5-

Indexed as

AzidesPyrimidinesAlkynesTetrazolesAlkynesAzidespyrimidinePyrimidinesTetrazolesazideCuAAC chemistrypyrido[3,2-d]pyrimidineSnArtautomeric equilibriumtetrazoletriazoleX-ray structure determination

Identifiers

PMID36431776

DOI10.3390/molecules27227675

PMCPMC9698326

OpenAlexW4308568214

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.