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
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
e32188Informations de copyright
© 2024 The Authors.
Déclaration de conflit d'intérêts
The authors declare no conflict of interest.