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Structural studies of benzophenanthridine alkaloid free bases by NMR spectroscopy
Autoři | |
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Rok publikování | 2002 |
Druh | Článek v odborném periodiku |
Časopis / Zdroj | Magnetic Resonance in Chemistry |
Fakulta / Pracoviště MU | |
Citace | |
www | http://www3.interscience.wiley.com/cgi-bin/abstract/88512831/START |
Obor | Organická chemie |
Klíčová slova | NMR; 1H NMR; 13C NMR; benzophenanthridine alkaloids; free base formation; GHMBC; GSQMBC; pseudobases |
Popis | The free bases of eight quaternary benzo[c]phenanthridine alkaloids were investigated by 1H and 13C NMR spectroscopy. The pseudobases (the 6-hydroxy-5,6-dihydro derivatives) were found to be the only products of the alkalization in DMSO-d6 solution. In less polar solvents the formation of the bimolecular aminoacetal structure is preferred. In biological systems, free bases of the alkaloids are assumed to adopt the pseudobase structure. |
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