## Abstract ^13^C NMR chemical shifts for trimethylene sulphite and 35 derivatives are presented. From the magnitudes of the β shifts it has been possible to establish chemical shift additivity relationships for a series of compounds. The results are discussed in terms of probable conformations in
Chemistry of the SO bond. 11—carbon-13 and oxygen-17 nuclear magnetic resonance studies of stereoisomerism in 1,3,2-dioxathiepanes
✍ Scribed by Desmond G. Hellier; H. Glendon Liddy
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- English
- Weight
- 426 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
The stereoisomerism of some methyl-substituted 1,3,2-dioxathiepanes has been investigated by I3C and * '0 NMR spectroscopy. The effects of substituents on the conformational equilibria of the seven-membered rings are discussed and compared with those for six-membered ring sulphites.
📜 SIMILAR VOLUMES
## Abstract The influence of substituents in a new series of 2__H__‐thiopyrans, 2__H__‐thiopyran‐2‐ones (thiones) and their thiazine analogues is examined by means of carbon (^13^C) and nitrogen (^15^N) NMR. A linear relationship is shown to exist between the chemical shifts (δ~13C~ or δ~15N~) of t