𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Stereodivergent routes from tyrosine to the 7-(R) and 7-(S) diastereomers of the 7-hydroxy-2,3,7,7a-tetrahydroindole ring found in gliotoxin

✍ Scribed by Todd C Henninger; Michal Sabat; Richard J Sundberg


Publisher
Elsevier Science
Year
1996
Tongue
French
Weight
713 KB
Volume
52
Category
Article
ISSN
0040-4020

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Ring-chain tautomerism provides a route
✍ Langschwager, Wolf ;Hoffmann, H. Martin R. πŸ“‚ Article πŸ“… 1995 πŸ› John Wiley and Sons 🌐 English βš– 605 KB

tautomer I 4-Oxocarboxylic acids I Keto-cyclol tautomerism (2-Oxocyclohexyl)acetic acid 10 was converted into bicyclic alkoxy y-lactones 12a-d via intermediate chloro lactone 11 and alkanolysis. Similarly, lactones 15a, b and 18 were prepared. In contrast, simple ring-chain tautomerism directly affo

Synthesis of Mono- and Sesquiterpenoids,
✍ Yajima, Arata ;Takikawa, Hirosato ;Mori, Kenji πŸ“‚ Article πŸ“… 2006 πŸ› John Wiley and Sons 🌐 English βš– 749 KB

## Abstract The structure of the antibacterial sesquiterpene from __Premna oligotricha__ was shown to be not 1 but 2 (relative stereochemistry) by the unambiguous synthesis of both (Β±)‐1 and (Β±)‐2.