Evidence map›Paper›PMID 28485608›Full record

ArticleOrganic letters2017

Direct Regioselective Synthesis of Tetrazolium Salts by Activation of Secondary Amides under Mild Conditions.

Veronica Tona, Boris Maryasin, Aurélien de la Torre, Josefine Sprachmann, Leticia González, Nuno Maulide

Open access · hybridAbstract read
In one paragraph

Article in Organic letters, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

4 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. Article
  3. Chemoselective Intermolecular Cross-Enolate-Type Coupling of Amides.Journal of the American Chemical Society · 2017
    Article
  4. 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

6 authors at 1 institution in 1 country.

Veronica TonaUniversity of Vienna , Institute of Organic Chemistry, Währinger Strasse 38, 1090 Vienna, Austria.
Boris MaryasinUniversity of Vienna , Institute of Organic Chemistry, Währinger Strasse 38, 1090 Vienna, Austria.
Aurélien de la TorreUniversity of Vienna , Institute of Organic Chemistry, Währinger Strasse 38, 1090 Vienna, Austria.
Josefine SprachmannUniversity of Vienna , Institute of Organic Chemistry, Währinger Strasse 38, 1090 Vienna, Austria.
Leticia GonzálezUniversity of Vienna , Insitute of Theoretical Chemistry, Währinger Strasse 17, 1090 Vienna, Austria.ORCID 0000-0001-5112-794X
Nuno MaulideUniversity of Vienna , Institute of Organic Chemistry, Währinger Strasse 38, 1090 Vienna, Austria.ORCID 0000-0003-3643-0718
University of Vienna · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tetrazolium salts are biologically active molecules that have found broad applications in biochemical assays. A regioselective synthesis of tetrazolium salts is described through a formal (3 + 2) cycloaddition. The possibility of employing simple amides and azides as starting material and the mild conditions allow a broad functional group tolerance.

Identifiers

PMID28485608
PMCPMC5442602
OpenAlexW2612931736

What OpenQuestion holds

Textmetadata
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.