The intramolecular S
Diterpenoids
Intramolecule S(N)2 reaction
Isodon
Isodon amethystoides
Tautomer
Journal
Fitoterapia
ISSN: 1873-6971
Titre abrégé: Fitoterapia
Pays: Netherlands
ID NLM: 16930290R
Informations de publication
Date de publication:
21 Dec 2023
21 Dec 2023
Historique:
received:
25
10
2023
revised:
14
12
2023
accepted:
16
12
2023
medline:
24
12
2023
pubmed:
24
12
2023
entrez:
23
12
2023
Statut:
aheadofprint
Résumé
As our ongoing searching for the bioactive natural terpenoids, nine ent-kauranoids (1-9), including three previously undescribed ones (1, 2, and 9), were isolated from the aerial parts of Isodon amethystoides. Their structures were elucidated on the basis of spectroscopic data analysis, including NMR, MS, and ECD. Compounds 1 and 2 were a pair of tautomeric compounds, which was confirmed by the HPLC analysis and low temperature NMR testing. The underlying mechanism of the tautomer was proposed as an intramolecular S
Identifiants
pubmed: 38141880
pii: S0367-326X(23)00363-5
doi: 10.1016/j.fitote.2023.105788
pii:
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
105788Informations de copyright
Copyright © 2023. Published by Elsevier B.V.