Synthesis and structural study of new substituted chiral sulfamoyl oxazolidin-2-ones
β Scribed by Carole Barbey; Radia Bouasla; Malika Berredjem; Nathalie Dupont; Pascal Retailleau; Nour-Eddine Aouf; Marc Lecouvey
- Book ID
- 119375683
- Publisher
- Elsevier Science
- Year
- 2012
- Tongue
- French
- Weight
- 667 KB
- Volume
- 68
- Category
- Article
- ISSN
- 0040-4020
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
A series of three 5,5-diaryl substituted oxazolidin-2-ones (diphenyl, dinaphthyl and ditolyl) have been prepared and shown to be particularly effective chiral auxiliaries to afford high yields and diastereoselectivities for alkylation and azidations of their N-acyl derivatives. The 5,5-ditolyl oxazo
## 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, please click on HTML or PDF.
## Abstract A series of new chiral N,Nβ²βsulfonyl bisβoxazolidinβ2βones were synthesized starting from 2βaminoalcohols, sulfuryl chloride, and diethyl carbonate. This method utilizes natural amino acids as a source of chirality for the preparation of oxazolidinones. Β© 2006 Wiley Periodicals, Inc. He