The title compounds (2 and 4) obtained by the diastereoselective hydrogenation of the corresponding 1,2,3,6-tetrahydrophosphinine oxides (1 and 3) were subjected to a detailed quantum chemical study. The possible chair conformers were calculated at the HF/6-31G \* level of theory, according to which
On the NMR spectrum of 1,3-oxathiane-3-oxide: A contrast between the conformational preference of the sulphinyl oxygen in 1,3-oxathiane-3-oxide and in 1,3-dithiane-1-oxides
✍ Scribed by Knut Bergesen; Michael J. Cook; Alan P. Tonge
- Publisher
- John Wiley and Sons
- Year
- 1974
- Tongue
- English
- Weight
- 182 KB
- Volume
- 6
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
The 100 MHz spectrum of 1,3‐oxathiane‐3‐oxide is reported. Parameters obtained from first order analyses are interpreted in terms of an absence of a conformational preference of the SO bond at 38°C, but an axial preference at low temperatures. The behaviour contrasts with that found previously in the 1,3‐dithiane‐1‐oxide series.
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