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
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