The molecular conformation of phthalideisoquinoline derivatives was studied by 'H NMR methods. For the qualitative determination of the conformational preferences, proton relaxation times, 1D and 2D NOE experiments were applied. Our proposals were supported by the calculation of the effects of ring
A conformational study on some catecholamine derivatives
β Scribed by Brussee, J. ;Erkelens, C. ;Jansen, A. C. A. ;Gerritsma, K. W.
- Publisher
- Springer
- Year
- 1980
- Tongue
- Dutch
- Weight
- 435 KB
- Volume
- 2
- Category
- Article
- ISSN
- 1573-739X
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