Evidence map›Paper›PMID 37461839›Full record

ArticleChemistry (Weinheim an der Bergstrasse, Germany)2023

Asymmetric Transfer Hydrogenation as a Key Step in the Synthesis of the Phosphonic Acid Analogs of Aminocarboxylic Acids.

Tamara Dinhof, Thomas Kalina, Toda Stanković, Kristóf Braunsteiner, Philipp Rohrbach, Ertan Turhan, Andreas Gradwohl, Artur Königshofer, Jeannie Horak, Katharina Pallitsch

Open access · hybridAbstract read
In one paragraph

Article in Chemistry (Weinheim an der Bergstrasse, Germany), 2023. 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
0.6field-weighted citation impact, top 37% 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, 4 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

10 authors at 2 institutions in 2 countries.

Tamara DinhofInstitute of Organic Chemistry, Faculty of Chemistry, University of Vienna, Währingerstraße 38, 1090, Vienna, Austria.
Thomas KalinaInstitute of Organic Chemistry, Faculty of Chemistry, University of Vienna, Währingerstraße 38, 1090, Vienna, Austria.
Toda StankovićInstitute of Organic Chemistry, Faculty of Chemistry, University of Vienna, Währingerstraße 38, 1090, Vienna, Austria.
Kristóf BraunsteinerInstitute of Organic Chemistry, Faculty of Chemistry, University of Vienna, Währingerstraße 38, 1090, Vienna, Austria.
Philipp RohrbachInstitute of Organic Chemistry, Faculty of Chemistry, University of Vienna, Währingerstraße 38, 1090, Vienna, Austria.
Ertan TurhanInstitute of Organic Chemistry, Faculty of Chemistry, University of Vienna, Währingerstraße 38, 1090, Vienna, Austria.
Andreas GradwohlVienna Doctoral School in Chemistry (DoSChem), University of Vienna, Währingerstraße 42, 1090, Vienna, Austria.
Artur KönigshoferInstitute of Organic Chemistry, Faculty of Chemistry, University of Vienna, Währingerstraße 38, 1090, Vienna, Austria.
Jeannie HorakDivision of Metabolic and Nutritional Medicine, Dr. von Hauner Children's Hospital, Ludwig Maximilians University Munich Medical Center, Lindwurmstraße 4, 80337, Munich, Germany.
Katharina PallitschInstitute of Organic Chemistry, Faculty of Chemistry, University of Vienna, Währingerstraße 38, 1090, Vienna, Austria.ORCID https://orcid.org/0000-0003-2648-1044
University of Vienna · ATLudwig-Maximilians-Universität München · DE

Funding

Austrian Science Fund P27987
6 · The paper itself

Abstract

α-Aminophosphonic acids have a remarkably broad bioactivity spectrum. They can function as highly efficient transition state mimics for a variety of hydrolytic and angiotensin-converting enzymes, which makes them interesting target structures for synthetic chemists. In particular, the phosphonic acid analogs to α-aminocarboxylic acids (P

Indexed as

OrganophosphonatesPhosphorous AcidsHydrogenationMolecular StructureStereoisomerismOrganophosphonatesphosphonic acidPhosphorous Acidsaminophosphonatesasymmetric transfer hydrogenationdeuterationhydroxyphosphonates

Identifiers

PMID37461839
PMCPMC10947287
OpenAlexW4384625870

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.