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

Hydrogenation Molecular Structure Phosphorous Acids / chemistry Organophosphonates / chemistry Stereoisomerism
aminophosphonates asymmetric transfer hydrogenation deuteration hydroxyphosphonates

Journal

Chemistry (Weinheim an der Bergstrasse, Germany)
ISSN: 1521-3765
Titre abrégé: Chemistry
Pays: Germany
ID NLM: 9513783

Informations de publication

Date de publication:
22 Dec 2023
Historique:
received: 10 07 2023
medline: 25 12 2023
pubmed: 18 7 2023
entrez: 18 7 2023
Statut: ppublish

Résumé

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

Identifiants

DOI: 10.1002/chem.202302171 PMID: 37461839
pubmed: 37461839
doi: 10.1002/chem.202302171
doi:

Substances chimiques

phosphonic acid 13598-36-2
Phosphorous Acids 0
Organophosphonates 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e202302171

Subventions

Organisme : Austrian Science Fund
ID : P27987

Informations de copyright

© 2023 The Authors. Chemistry - A European Journal published by Wiley-VCH GmbH.

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Auteurs

Tamara Dinhof (T)

Institute of Organic Chemistry, Faculty of Chemistry, University of Vienna, Währingerstraße 38, 1090, Vienna, Austria.
Vienna Doctoral School in Chemistry (DoSChem), University of Vienna, Währingerstraße 42, 1090, Vienna, Austria.

Thomas Kalina (T)

Institute of Organic Chemistry, Faculty of Chemistry, University of Vienna, Währingerstraße 38, 1090, Vienna, Austria.

Toda Stanković (T)

Institute of Organic Chemistry, Faculty of Chemistry, University of Vienna, Währingerstraße 38, 1090, Vienna, Austria.

Kristóf Braunsteiner (K)

Institute of Organic Chemistry, Faculty of Chemistry, University of Vienna, Währingerstraße 38, 1090, Vienna, Austria.

Philipp Rohrbach (P)

Institute of Organic Chemistry, Faculty of Chemistry, University of Vienna, Währingerstraße 38, 1090, Vienna, Austria.

Ertan Turhan (E)

Institute of Organic Chemistry, Faculty of Chemistry, University of Vienna, Währingerstraße 38, 1090, Vienna, Austria.
Vienna Doctoral School in Chemistry (DoSChem), University of Vienna, Währingerstraße 42, 1090, Vienna, Austria.

Andreas Gradwohl (A)

Vienna Doctoral School in Chemistry (DoSChem), University of Vienna, Währingerstraße 42, 1090, Vienna, Austria.
Institute of Inorganic Chemistry, Faculty of Chemistry, University of Vienna, Josef-Holaubek-Platz 2, 1090, Vienna, Austria.

Artur Königshofer (A)

Institute of Organic Chemistry, Faculty of Chemistry, University of Vienna, Währingerstraße 38, 1090, Vienna, Austria.

Jeannie Horak (J)

Division of Metabolic and Nutritional Medicine, Dr. von Hauner Children's Hospital, Ludwig Maximilians University Munich Medical Center, Lindwurmstraße 4, 80337, Munich, Germany.

Katharina Pallitsch (K)

Institute of Organic Chemistry, Faculty of Chemistry, University of Vienna, Währingerstraße 38, 1090, Vienna, Austria.
ORCID: 0000-0003-2648-1044

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Classifications MeSH

questionsmedicales.fr › Métabolisme › Hydrogénation › Asymmetric Transfer Hydrogenation as a Key...
questionsmedicales.fr › Phénomènes chimiques › Structure moléculaire › Asymmetric Transfer Hydrogenation as a Key...
questionsmedicales.fr › Produits chimiques inorganiques › Composés du phosphore › Acides du phosphore › Acides phosphoreux › Asymmetric Transfer Hydrogenation as a Key...
questionsmedicales.fr › Composés chimiques organiques › Composés organiques du phosphore › Phosphonates › Asymmetric Transfer Hydrogenation as a Key...
questionsmedicales.fr › Phénomènes chimiques › Phénomènes de chimie organique › Isomérie › Stéréoisomérie › Asymmetric Transfer Hydrogenation as a Key...