## Abstract The ^1^H and ^13^C NMR data for 3‐azabicyclo[3.3.1]nonanes with OH and OMe substituents at C‐6 and C‐9 were measured using 1D (DEPT) and 2D (COSY, HSQC, HMBC, NOESY) experiments. Comparison of this NMR data illustrates the effects of stereochemistry and substitution at these positions.
13C Nuclear magnetic resonance spectra of 2-substituted bicyclo(3.3.1)nonan-9-ones
✍ Scribed by A. Heumann; H. Kolshorn
- Publisher
- Elsevier Science
- Year
- 1975
- Tongue
- French
- Weight
- 517 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0040-4020
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📜 SIMILAR VOLUMES
## Abstract The ^13^C NMR spectra of 48 differently substituted chalcones (1,3‐diphenylprop‐2 enones) have been recorded and the results are discussed. The data will be useful in the identification of new/natural chalcones.
## Abstract The ^13^C NMR spectra of 26 substituted 2‐azabicyclo[3.3.1]nonan‐7‐ones are reported, providing a diagnostic method for the stereochemical elucidation of the relative configuration of these products.
## Abstract Carbon‐13 NMR spectra of solid polycrystalline bicyclo[3.3.1]nonan‐9‐one and adamantanone have been measured at 315K. The relatively narrow ^13^C linewidths observed for these solids, together with measured spin‐lattice relaxation times, indicate that both these solids are orientational