𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Stereospecific allylsilane reactions: a total synthesis of dihydronepetalactone

✍ Scribed by Ian Fleming; Nicholas K Terrett


Publisher
Elsevier Science
Year
1984
Tongue
French
Weight
146 KB
Volume
25
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Total synthesis of (Β±)-Ξ±-allokainic acid
✍ Hendrik H Mooiweer; Henk Hiemstra; W.Nico Speckamp πŸ“‚ Article πŸ“… 1991 πŸ› Elsevier Science 🌐 French βš– 914 KB

A total synthesis of racemic a-allokainic acid is described, which starts from allylsilane 8 and methoxy-or chloroglycine derivative 9, and proceeds fully stereoselectively in nine steps and 1.1% overall yield. Key steps are the intermolecular N-acyliminium ion coupling of 8 with 9 and an intramolec

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.