Evidence map›Paper›PMID 35604200›Full record

ArticleChemistry (Weinheim an der Bergstrasse, Germany)2022

Carboxylate Catalyzed Isomerization of β,γ-Unsaturated N-Acetylcysteamine Thioesters.

Saara Riuttamäki, Gergely Laczkó, Ádám Madarász, Tamás Földes, Imre Pápai, Anton Bannykh, Petri M Pihko

Open access · greenAbstract read
In one paragraph

Article in Chemistry (Weinheim an der Bergstrasse, Germany), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-weighted citation impact, top 31% 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

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Carboxylate-CatalyzedOrganic letters · 2024
    Article
  2. Carboxylate Catalysis: A CatalyticThe Journal of organic chemistry · 2023
    Article
  3. 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

7 authors at 2 institutions in 2 countries.

Saara RiuttamäkiDepartment of Chemistry, University of Jyväskylä, P.O. Box 35, 40014, Jyväskylä, Finland.
Gergely LaczkóInstitute of Organic Chemistry, Research Centre for Natural Sciences, Magyar tudósok körútja 2, 1117, Budapest, Hungary.
Ádám MadarászInstitute of Organic Chemistry, Research Centre for Natural Sciences, Magyar tudósok körútja 2, 1117, Budapest, Hungary.
Tamás FöldesInstitute of Organic Chemistry, Research Centre for Natural Sciences, Magyar tudósok körútja 2, 1117, Budapest, Hungary.
Imre PápaiInstitute of Organic Chemistry, Research Centre for Natural Sciences, Magyar tudósok körútja 2, 1117, Budapest, Hungary.
Anton BannykhDepartment of Chemistry, University of Jyväskylä, P.O. Box 35, 40014, Jyväskylä, Finland.
Petri M PihkoDepartment of Chemistry, University of Jyväskylä, P.O. Box 35, 40014, Jyväskylä, Finland.ORCID http://orcid.org/0000-0003-0126-0974
Institute of Organic Chemistry · HUUniversity of Jyväskylä · FI

Funding

Academy of Finland 297874Academy of Finland 307624Academy of Finland 322899NKFIH Hungary K-112028
6 · The paper itself

Abstract

We demonstrate herein the capacity of simple carboxylate salts - tetrametylammonium and tetramethylguanidinium pivalate - to act as catalysts in the isomerization of β,γ-unsaturated thioesters to α,β-unsaturated thioesters. The carboxylate catalysts gave reaction rates comparable to those obtained with DBU, but with fewer side reactions. The reaction exhibits a normal secondary kinetic isotope effect (k

Indexed as

Carboxylic AcidsIsotopesCatalysisIsomerismKineticsCarboxylic AcidsIsotopesbase catalysiscarboxylatesenolatesisomerizationkinetic isotope effectsreaction mechanismthioesters

Identifiers

PMID35604200
PMCPMC9541288
OpenAlexW4281293625

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.