𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Facile synthesis of α-hydroxy carbonyl compounds by enolate oxidation with dimethyldioxirane

✍ Scribed by Kevin R. Guertin; Tak-Hang Chan


Publisher
Elsevier Science
Year
1991
Tongue
French
Weight
289 KB
Volume
32
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

✦ Synopsis


The dwzt oxldatron of enolates with &methylchoxirane ( as a solunon m acetone ) provides the ahydroxy &nvanves m excellent yield

The converSlon of enohzable ketones to their correspondmg a-hydroxy denvatlves 1s an important synthenc transformanon and has received a great deal of attennon la2 The class~al method of acluevmg tis transformation


📜 SIMILAR VOLUMES


Facile synthesis of silyl enol ethers by
✍ Yoshio Ishino; Yoshio Kita; Hirofumi Maekawa; Toshinobu Ohno; Yasuhiro Yamasaki; 📂 Article 📅 1999 🏛 Elsevier Science 🌐 French ⚖ 225 KB

Treatment of aliphatic carbonyl compounds with trimethyisilyl chloride with Mg turning for Grignard reaction without any pre-treatmem in N,N-dimethylformamide at room temperature brought about highly facile, effective and stereoselective coupling to give the corresponding silyl enol ethers in good y