Abstract
An ether extract of Wikstroemia montícola (Thymelaeaceae) yielded, upon further fractionation, a tic-homogeneous mixture. The resolution of this mixture by reversed phase hplc gave six daphnane diterpenes: wikstrotoxins A (1), B (3), C (5), and D (6), huratoxin (2), and excoecariatoxin (4). The identities of wikstrotoxins A-D, which are new, were established by spectral properties. For the first time, 13C-nmr data are given for 2.
Original language | English (US) |
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Pages (from-to) | 675-680 |
Number of pages | 6 |
Journal | Journal Of Natural Products |
Volume | 46 |
Issue number | 5 |
DOIs | |
State | Published - Sep 1983 |
ASJC Scopus subject areas
- Analytical Chemistry
- Molecular Medicine
- Pharmacology
- Pharmaceutical Science
- Drug Discovery
- Complementary and alternative medicine
- Organic Chemistry