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-
13C- and 1H-NMR. Assignments for colchicine derivatives
✍ Scribed by Charles D. Hufford; Hans-Georg Capraro; Arnold Brossi
- Publisher
- John Wiley and Sons
- Year
- 1980
- Tongue
- German
- Weight
- 412 KB
- Volume
- 63
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The ^13^C‐NMR. spectra of a number of colchicine derivatives are given comprising examples of the normal series (4→10), iso series (11→16) and colchicine series (17), which were either reported in the literature or obtained by partial synthesis or degradation reactions. The ^13^C‐NMR. assignments were made by comparisons with known compounds and selective single‐frequency offresonance decoupling experiments. Selective proton decoupling experiments have also allowed assignments of the H—C(11) and H—C(12) protons of the iso and colchicine series.
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