## Abstract Some 2‐arylsulphonylamido‐2‐thiono‐5‐methyl‐1,3,2‐dioxaphospholanes (1), containing two chiral centres, give NMR spectra in which splittings of the ^1^H and ^13^C signals of the 5‐methyl substituent and of the ^31^P signal indicate that they exist in an approximately 70:30% ratio of two
1H, 13C, 31P NMR and conformational study of 7-membered ring organophosphorus compounds. 1,3,2-dioxaphosphepanes
✍ Scribed by A. C. Guimaraes; J. B. Robert; C. Taieb; J. Tabony
- Publisher
- John Wiley and Sons
- Year
- 1978
- Tongue
- English
- Weight
- 721 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
The *H, '% and 31P NMR data of several Z-R-2-thiono-1,3-dioxa organophosphorus molecules with 7-membered rings [R = 43, OC6H,, C,H,, CH3, N(CH,),] are reported. The conformation of the 7-membered ring is discussed by reference to the 'J(P0CH) coupling constants which are compared with those observed in 6-membered 1,3,2-dioxaphosphorinanes. It is shown that caution must be exercised in using the 'J(POCH) angular dependence as a stereochemical tool. The 31P spin lattice relaxation times of some of these 7-membered rings have been measured and the values are discussed.
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