## Abstract The carbon shifts of the Iboga‐type alkaloids catharanthine, voacangine, coronaridine, ibogaine, dihydrocatharanthine and epiibogamine were recorded and correlated with the conformation of the natural bases. A ^13^C‐NMR. analysis of heyneanine determined its C(19) configuration and a si
13C-NMR. Spectroscopy of Naturally Occurring Substances. XXXII. Vincaleucoblastine and related alkaloids
✍ Scribed by Ernest Wenkert; Edward W. Hagaman; Bansi Lal; Gerald E. Gutowski; Allen S. Katner; Jean C. Miller; Norbert Neuss
- Publisher
- John Wiley and Sons
- Year
- 1975
- Tongue
- German
- Weight
- 918 KB
- Volume
- 58
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
The total assignment of the ^13^C‐shifts of the complex Vinica rosea L. alkaloids vincaleucoblastine, leurosidine and leurosine and of a synthetic isomer of the latter is presented. The structure of leurosidine is corrected and a tentative structure for the acid‐catalyzed product of isomerization of leurosine is proposed.
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