H and 13 C NMR spectroscopic data for 5a-androstanes and halo-5a-androstanes with different substituents at positions C-3, C-9, C-11 and C-17 were examined and assigned by a combination of 1D and 2D NMR experiments. The substituent effects on the 13 C chemical shifts were compared with those of epi-
Tautomerism and 1H and 13C NMR assignment of methyl derivatives of 9-hydroxyphenalenone
✍ Scribed by Brian Honeyman; Charles Spalding; Dell Jensen Jr.; Robert C. Haddon
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 133 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.1706
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