## Abstract Carbon and proton chemical shifts are used, together with interproton coupling constants, to establish the preferred localisation of charge in protonated eucarvone. Comparison with the HΓΌckel values suggests predominant residence of the FSO~3~βcounter ion near Cβ3.
β¦ LIBER β¦
Ring inversion in eucarvone
β Scribed by E. Cuthbertson; D.D. MacNicol
- Publisher
- Elsevier Science
- Year
- 1974
- Tongue
- French
- Weight
- 100 KB
- Volume
- 15
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Considerable attention1 has been directed towards the determination of conformations and conformational mobilities of simple seven-membered carbocycles which are fully saturated or have one or three endocyclic double bonds. On the other hand, the corresponding unfused systems possessing two double bonds in the ring have received little attention, though molecular mechanics calculations ' on cyclohepta-1,3-diene (I) indicate an extremely high degree of molecular mobility for this molecule.
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