𝔖 Bobbio Scriptorium
✦   LIBER   ✦

High yield stereospecific total synthesis of vincamine

✍ Scribed by Herrmann, J. L.; Cregge, R. J.; Richman, J. E.; Semmelhack, C. L.; Schlessinger, R. H.


Book ID
127256952
Publisher
American Chemical Society
Year
1974
Tongue
English
Weight
217 KB
Volume
96
Category
Article
ISSN
0002-7863

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


High yield stereospecific total synthesi
✍ J.L. Hermann; G.R. Kierczykowski; S.E. Normandin; R.H. Sclessinger πŸ“‚ Article πŸ“… 1976 πŸ› Elsevier Science 🌐 French βš– 132 KB

## Eburnamomne (1) and eburnamlne (;?) are pentacycllc lndole alkaloids Isolated from Hunterza ebxrnea Plchon (Apocyanaceae) ' Eburnamomne is useful as a cerebrovsscular agent,2 and therefore, is of interest with respect to efficient total synthesis ' Herein, we descnbe a reglospeciflc alkylation

The Total Synthesis of Vincamine
✍ Kuehne, Martin E. πŸ“‚ Article πŸ“… 1964 πŸ› American Chemical Society 🌐 English βš– 139 KB
Stereospecific total synthesis of cycloe
✍ Edward Y. Chen πŸ“‚ Article πŸ“… 1982 πŸ› Elsevier Science 🌐 French βš– 226 KB

A stereospecific sequence from the allylic alcohol 3 to the new anti-biotic, cycloeudesmol 2, in 9 steps (21.7% overall yield) is described.