𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis of 3-ω-epoxido farnesyl indoles, intermediates in the biogenesis of sesquiterpenic indole alkaloids

✍ Scribed by Catherine Mirand; Michèle Döé de Maindreville; Jean Lévy


Book ID
104228856
Publisher
Elsevier Science
Year
1985
Tongue
French
Weight
222 KB
Volume
26
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Synthesis of 3-(indol-2-yl)-propenoate d
✍ Patrick D Bailey; Sean P Hollinshead 📂 Article 📅 1987 🏛 Elsevier Science 🌐 French ⚖ 228 KB

~ A simple three step route to 3-(indol-2-yl)--propenoate derivatives of tryptamine has been developed, involving the base-induced ring-opening of protected tetrahydro-8-carbolines that result from a modified Pictet-Spengler reaction. Several recent syntheses of indole alkaloids have utilised Z-prop

Aldehyde Intermediates in the Synthesis
✍ Arto Tolvanen; David Din Belle; Mauri Lounasmaa 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 German ⚖ 394 KB

## Abstract The synthesis of aldehyde intermediates suitable for the preparation of indole alkaloids of the tacamine (1) type is described. The four possible aldehydes 4–7 were prepared from methyl 5‐ethylnicotinate (8) in a few simple steps using a base‐catalyzed epimerization as the final step (_