Antitumor Sesquiterpenes from Euonymus nanoides
✍ Scribed by Hong Wang; Xuan Tian; Yuanjiang Pan
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- German
- Weight
- 93 KB
- Volume
- 86
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The isolation, structure elucidation, and antitumor activity of four new sesquiterpene polyol esters, i.e., of 6__α__,13‐bis(acetyloxy)‐9__β__‐(cinnamoyloxy)‐1__β__‐(furan‐3‐ylcarbonyl)oxy]‐4__α__‐hydroxy‐β‐dihydroagarofuran (1), 13‐(acetyloxy)‐9__β__‐(benzoyloxy)‐4__α__‐hydroxy‐1__β__,6__α__‐bis[(2‐methylbutanoyl)oxy]‐β‐dihydroagarofuran (2), 1__β__,6__α__,13‐ tri(acetyloxy)‐9__β__‐(cinnamoyloxy)‐4__α__‐hydroxy‐β‐dihydroagarofuran (3), and 6__α__,13‐bis(acetyloxy)‐9__β__‐(benzoyloxy)‐4__α__‐hydroxy‐1__β__‐[(2‐methylbutanoyl)oxy]‐β‐dihydroagarofuran (4), and of five known sesquiterpene polyol esters 5–9 from the seed oil of Euonymus nanoides Loes. are reported (β‐dihydroagarofuran=octahydro‐2,2,5a,9‐tetramethyl‐2__H__‐3,9a‐methano‐1‐benzoxepin).
📜 SIMILAR VOLUMES
## Abstract Three new macrocyclic __β__‐dihydroagarofuran‐type sesquiterpene pyridine alkaloids, fortuneines A (**1**), B (**2**), and C (**3**), together with the four known alkaloids wilfornine E (**4**), aquifoliunine E‐I (**5**), euoverrine B (**6**), and euojaponine I (**7**), were isolated fr