## Abstract A series of 2‐anilino‐2‐thio‐1,3,2‐oxazaphospholanes derived from ephedrine has been synthesized and conformationally studied by proton NMR and X‐ray crystallography. The NMR data can be interpreted in terms of twist‐envelope conformations in which the anilino substituents on phosphorus
Synthesis of stereoisomeric substituted 1,3,2-oxazaphospholanes
✍ Scribed by N. V. Kaz'mina; I. L. Knunyants
- Book ID
- 112436151
- Publisher
- Springer
- Year
- 1967
- Tongue
- English
- Weight
- 231 KB
- Volume
- 16
- Category
- Article
- ISSN
- 1573-9171
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📜 SIMILAR VOLUMES
Although reactions between (-)ephedrine E2-(S)-methylamino-l-(R)-phenylpropan-l-017 and RPOC12 (R = Cl, alkyl, aryl, alkoxy, aryloxy) can in principle afford pairs of 1,3,2-oxazaphospholanes eyimeric at phosphorus, most reports describe only one product from highly stereoselective reactions.
## Abstract Dialkylamino‐3,4‐dimethyl‐5‐phenyl‐1,3,2‐oxazaphospholane sulfides (where the alkyl is an isopropyl, ethyl or methyl group) was obtained by sulfurization of the respective phospholanes. The structures of these compounds were determined by X‐ray crystal structure analysis. Five‐membered