**The Structure of the Alkaloid Juliprosopine from Prosopis juliflora A. Dc.** A new alkaloid, juliprosopine, has been isolated from __Prosopis__ __juliflora__ A. Dc. __(Leguminosae)__, for which structure **1** is proposed. The piperidine moiety could be elucidated on the basis of spectroscopic da
Die Struktur des Curare-Alkaloides Calebassinin-1 183. Mitteilung uber organische Naturstoffe
✍ Scribed by Armin Guggisberg; Roland Prewo; Jost H. Bieri; Manfred Hesse
- Publisher
- John Wiley and Sons
- Year
- 1982
- Tongue
- German
- Weight
- 557 KB
- Volume
- 65
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
✦ Synopsis
The Structure of the Calabash Curare Alkaloid Calebassinine‐1
The quaternary alkaloid calebassinine, isolated 1947 from Calabash Curare. has now been separated into calebassinine‐1 and ‐2. X‐ray structure determination of calebassinine‐1 led to structure 2 with relative configuration. A possible biogenetic pathway from 2,16‐dihydroakuammicine (3) as well as its pyrolytic decomposition to 3‐ethylpyridine (9), the quinoline derivative 8, methylchloride and norcale bassinine‐1 are discussed.
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**The Absolute Configuration of Macroline, a Degradation Product of the Alkaloid Villalstonine** The absolute configuration of macroline **(1)**, a degradration product of villalstonine **(2)**, was determined. The chemical degradation of **1** gave a mixture of (–)‐(20__S__)‐20,21‐dihydro‐19‐desox
Sul?zmai.y. Treatment of the Calebash alkaloid C-calebassine (l), C,PH48N40,++. 2 X-, with hot mineral acid yielded the anhydro-isocalebassine acid adduct 3H, with the formula C,H,,N,O+ ++ ' 3 X-. H,O. This mas converted into anhydro-isocalebassine methyl ether salts (4) C,,H,,N,O I-+. 2 X-. H,O wit