Diastereoselective formation of 2-aryl-3-arenesulfonyl 4-ethyl-1,3-oxazolidines: An X-ray crystallographic and 1H NMR study
✍ Scribed by G.Biju Kumar; Hetal.V Patel; Amrish C Shah; Markus Trenkle; Christine J Cardin
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- English
- Weight
- 318 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0957-4166
No coin nor oath required. For personal study only.
✦ Synopsis
N-Arylsulfonamides of (R)-and (S)-2-anfmo-l-butanol, on condensation with aromatic aldehydes produced diastereomerically pure 2-aryl-3-arenesulfonyl 4-ethyl-l,3oxazolidines. The absolute configurations of one enantiomeric pair have been determined from two fully refined X-ray structures, supplemented by nmr data.Copyrighi
📜 SIMILAR VOLUMES
## Abstract Ten new 1,2,4‐triazolo[3,4‐__b__]‐1,3,4‐thiadiazole derivatives were synthesized and their NMR spectra were analyzed by 1D and 2D NMR techniques (gCOSY, gHMBC, gHMQC). Copyright © 2001 John Wiley & Sons, Ltd.