Cargando…
Acid-Induced Rearrangement of Epoxygermacranolides: Synthesis of Furanoheliangolides and Cadinanes from Nobilin
The acid-induced rearrangement of three epoxyderivatives of nobilin 1, the most abundant sesquiterpene lactone in Anthemis nobilis flowers, was investigated. From the 1,10-epoxyderivative 2, furanoheliangolide 5 was obtained, while the 4,5-epoxy group of 3 did not react. Conversely, when the 3-hydro...
Autores principales: | De Mieri, Maria, Smieško, Martin, Ismajili, Isidor, Kaiser, Marcel, Hamburger, Matthias |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149915/ https://www.ncbi.nlm.nih.gov/pubmed/29258233 http://dx.doi.org/10.3390/molecules22122252 |
Ejemplares similares
-
Unravelling the Mode of Action of Furanoheliangolides through Total
Synthesis and Chemical Proteomics
por: Hoock, Joseph G. F., et al.
Publicado: (2021) -
Antitrypanosomal Activity of Sesquiterpene Lactones from Helianthus tuberosus L. Including a New Furanoheliangolide with an Unusual Structure
por: Galkina, Anna, et al.
Publicado: (2019) -
Identification of a Covalent Importin-5 Inhibitor,
Goyazensolide, from a Collective Synthesis of Furanoheliangolides
por: Liu, Weilong, et al.
Publicado: (2021) -
New Cadinane Sesquiterpenes from the Stems of Kadsura heteroclita
por: Cao, Liang, et al.
Publicado: (2019) -
A New Cadinane Sesquiterpene from the Marine Brown Alga Dictyopteris divaricata
por: Wen, Wei, et al.
Publicado: (2009)