Sesquiterpenoids from the Rhizome of Ligularia virgaurea
✍ Scribed by Xiao-Bai Sun; Yang-Jun Xu; Dong-Feng Qiu; Cheng-Shan Yuan
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- German
- Weight
- 88 KB
- Volume
- 90
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Two novel sesquiterpene dimers, compounds 1 and 2, were isolated from the rhizome of Ligularia virgaurea, together with the six known sesquiterpenoids 3–8. Their structures were established by physico‐chemical and spectroscopic methods, especially by means of 1D‐ and 2D‐NMR as well as HR‐MS analyses. A mechanism based on a classical Diels–Alder cyclization is proposed for the formation of the dimer 1 from the precursors 8 and the quinone form of 6 (Scheme).
📜 SIMILAR VOLUMES
## Abstract From the BuOH extract of the whole plant of __Ligularia virgaurea__ spp. __oligocephala__, a series of sesquiterpenes, sesquiterpene glycosides, and lignan glycosides were isolated, including the three new compounds (1__α__)‐1‐hydroxy‐8‐oxo‐eremophila‐6,9‐dien‐12‐oic acid (**1**), 8‐[(_
## Abstract Two new eremophilane‐type sesquiterpenoids eremophil‐6‐en‐11‐ol (**1**) and (7__α__,9__α__,10__α__)‐9,10‐epoxy‐eremophilan‐11‐ol (**2**), together with a known eremophilane‐type (6__α__,8__α__)‐6,8‐dihydroxyeremophil‐7(11)‐en‐12‐oic acid 12,8‐lactone (**3**) were isolated from the rhizo
## Abstract From the roots of __Ligularia virgaurea__, five new eremophilane‐type sesquiterpenes were isolated, including three new eremophilenolides, 6__β__‐(angeloyloxy)‐1__α__,8__β__,10__β__‐trihydroxyeremophil‐7(11)‐en‐12,8__α__‐olide (**1**), 6__β__‐(angeloyloxy)‐1__β__,10__β__‐epoxy‐8__β__‐et