C-3 alkoxymethylation of 4-oxo-1,4-dihydroquinoline 2-carboxylic acid esters

Alkoxyalkylation Amino acid catalysis Kynurenic acid Mannich reaction

Journal

Heliyon
ISSN: 2405-8440
Titre abrégé: Heliyon
Pays: England
ID NLM: 101672560

Informations de publication

Date de publication:
15 Jun 2024
Historique:
received: 14 03 2024
revised: 28 05 2024
accepted: 29 05 2024
medline: 17 6 2024
pubmed: 17 6 2024
entrez: 17 6 2024
Statut: epublish

Résumé

Esters of kynurenic acid, a known neuroprotective agent were reacted with cyclic amino acids to yield novel alkoxymethylated products under optimized reaction conditions. The importance of amino acid based (primary, secondary, biogenic and synthetic) organic additives was proven by the conduction of numerous test reactions. Thoroughly extended investigations, directly focusing on amino acid catalysis, which is an emerging and up-to-date field of catalysis and green chemical processes, have been conducted. The mechanism of the alkoxymethylation reaction was proposed and later the findings supported the hypothesis of the first

Identifiants

pubmed: 38882378
doi: 10.1016/j.heliyon.2024.e32188
pii: S2405-8440(24)08219-7
pmc: PMC11176925
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e32188

Informations de copyright

© 2024 The Authors.

Déclaration de conflit d'intérêts

The authors declare no conflict of interest.

Auteurs

Péter Simon (P)

Institute of Pharmaceutical Chemistry, University of Szeged, Eötvös u. 6, H-6720, Szeged, Hungary.

Bálint Lőrinczi (B)

Institute of Pharmaceutical Chemistry, University of Szeged, Eötvös u. 6, H-6720, Szeged, Hungary.

István Szatmári (I)

Institute of Pharmaceutical Chemistry, University of Szeged, Eötvös u. 6, H-6720, Szeged, Hungary.
HUN-REN SZTE Stereochemistry Research Group, University of Szeged, Eötvös u. 6, H-6720, Szeged, Hungary.

Classifications MeSH