## Abstract ^1^H NMR of the tricyclic molecule 3 ‐ Cyano ‐1,2,2‐ trimethyl ‐ 6 ‐ azatricyclo ‐[3.3.1.0^3,8^]non‐6‐ene does not permit the distinction between this structure and the other regioisomer that can be formed in a photochemically induced reaction. The elucidation of the structure was possi
Total assignment of the 1H and 13C NMR spectra of new 1-phenyl- and 1-cyano-substituted 3,3-dimethyl-2-thiatricyclo[3.2.1.16,8]nonane 2,2-dioxide through the application of two-dimensional NMR techniques
✍ Scribed by Robert Faure; Bernard Vacher; André Samat; Michel Chanon
- Publisher
- John Wiley and Sons
- Year
- 1987
- Tongue
- English
- Weight
- 320 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Total assignment of "C and 'H NMR spectra of the new compounds 1-cyano-and 1-phenyl-substituted 3,fdimethyl-2-thiatricycl0[3.2.l.l~~~]nonane 2,Z-dioxide was achieved using the concerted application of two-dimensional homonuclear and heteronuclear chemical shift correlations. This unequivocal structure determination rules out the formation of a six-membered ring during the intramolecular cyclization of the a-sulphonyl-C-centred radical originating from 5-endo-isopropylsulphonyl-5-exo-substituted norbornene.
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