Synthesis of N-acyl-β-aminoalcohols from N-acyloxazolidinones mediated by sodium azide
✍ Scribed by Abderrahim Bouzide; Gilles Sauvé
- Book ID
- 104250580
- Publisher
- Elsevier Science
- Year
- 2002
- Tongue
- French
- Weight
- 68 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
N-Acyl-b-aminoalcohols were obtained efficiently via a highly endocyclic cleavage of N-acyloxazolidinones mediated by sodium azide in methanol at 40°C.
📜 SIMILAR VOLUMES
## Abstract Several __N__‐acyl‐β‐hydroxyamino acids were prepared and treated with di‐__tert__‐butyl dicarbonate in the presence of 4‐(dimethylamino)pyridine, followed by treatment with __N__,__N__,__N′__,__N′__‐tetramethylguanidine to give the corresponding __N__‐acyldehydroamino acids in good to
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v