𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis of Three Jasmin Constituents via a Central Intermediate

✍ Scribed by Paul Dubs; Rita Stüssi

Publisher
John Wiley and Sons
Year
1978
Tongue
German
Weight
414 KB
Volume
61
Category
Article
ISSN
0018-019X

No coin nor oath required. For personal study only.

✦ Synopsis

Abstract

Syntheses of jasmone (1), methyl jasmonate (3) and γ‐jasmolactone (2) are reported, (Z)‐nona‐1, 6‐dien‐3‐one (4) serving as common intermediate.

📜 SIMILAR VOLUMES

Synthesis of a Central Intermediate in t
Synthesis of a Central Intermediate in the Biosynthesis of Di- and Trideoxysugars
✍ Müller, Thomas ;Schmidt, Richard R. 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 943 KB

## Abstract The synthesis of disodium (6‐deoxy‐α‐D‐__ribo__‐hexopyran‐3‐ulosyl) (2′‐deoxythymidin‐5′‐yl) diphosphate (1) is described. To this end, D‐glucose is transformed into known furanose derivative 2 possessing a 3‐__C__‐methylene group as latent functionality for 3‐ulose generation. From 2,

Synthesis of Eburnamine, Isoeburnamine,
Synthesis of Eburnamine, Isoeburnamine, and Eburnamonine via a Spirocyclic Intermediate
✍ Tse-Lok Ho; Chun-Kuei Chen 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 German ⚖ 103 KB

## Abstract Racemic eburnamonine (**1**) was synthesized __via__ **6**, an intermediate possessing local symmetry. Cleavage of the cyclopentene subunit led to pentacyclic aldehydes **8a**/**8b** which on subsequent borohydride and __Wolff–Kishner__ reductions gave **12**. The final steps included a