I7O NMR chemical shifts of 2-oxo-1,3,2-dioxathiane and 13 of its methyl-substituted derivatives are reported. The chemical shifts depend strongly on temperature and to a much smaller extent on concentration. As a whole, however, they strongly support the predominance of chair conformations in these
β¦ LIBER β¦
Fragmentation and isomerization reactions of phenyl substituted 2-oxo-1,3,2-dioxathianes (trimethylene sulfites)
β Scribed by Robert J. Olsen; Timothy A. Lewis; Manish A. Mehta; Jeffrey G. Stack
- Book ID
- 112128297
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 1986
- Tongue
- English
- Weight
- 339 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0022-152X
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## Abstract Seven isomeric 4,5,6βtrimethylβ2βoxoβ1,3,2βdioxathians, __cis__β4β__trans__β6βdimethylβ__r__β2βoxoβ1,3,2βdioxathian and two isomeric 4,5,5,6βtetramethylβ2βoxoβ1,3,2βdioxathians were prepared and their ^1^H n.m.r. spectra analysed. The values of the vicinal coupling constants reported ea