𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Carbon-carbon bond fragmentation through oxidative electrolysis of carboxylic acids and its application to the synthesis of malyngolide

✍ Scribed by Wuts, Peter G. M.; Cheng, Minn Chang


Book ID
127098846
Publisher
American Chemical Society
Year
1986
Tongue
English
Weight
600 KB
Volume
51
Category
Article
ISSN
0022-3263

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


C-C bond formation on reduction of organ
✍ Yasuo Matsuki; Mitsuaki Kodama; Shô Itô 📂 Article 📅 1979 🏛 Elsevier Science 🌐 French ⚖ 200 KB

The bicyclic ethers obtained by the oxymercuration-demercuration reaction of linalool was found to be formed in the demercurotion step. The facile C-C bond formation is due to the proximity of Hg and the vinyl group in the organomercurial intermediate. Applying this process to epimanool a biomimetic

Asymmetric synthesis of α-substituted am
✍ Kolb, Michael ;Barth, Jacqueline 📂 Article 📅 1983 🏛 John Wiley and Sons 🌐 English ⚖ 1015 KB

## Abstract The asymmetric synthesis of α‐substituted α‐amino acids and propargylamines is described. As chiral auxiliary we used (__S__)‐(–)‐1‐dimethoxymethyl‐2‐methoxymethylpyrrolidine (SDMP, **1**). Treatment of the amino acids or amines with SDMP **1** afforded the corresponding amidines **C**,