Autocorrelated13c-13c double quantum coherence two-dimensional nmr spectroscopy: Utilization of a modified version of the technique as an adjunct in the total assignment of the1h- and13c-nmr spectra of the mutagen phenanthro[3,4-b]thiophene

1983 ◽  
Vol 20 (6) ◽  
pp. 1661-1669 ◽  
Author(s):  
M. J. Musmar ◽  
M. Robert Willcott ◽  
Gary E. Martin ◽  
Robert T. Gampe ◽  
Masatomo Iwao ◽  
...  
1990 ◽  
Vol 68 (2) ◽  
pp. 272-277 ◽  
Author(s):  
Torbjörn Drakenberg ◽  
Peter Brodelius ◽  
Deane D. McIntyre ◽  
Hans J Vogel

The 1H and 13C NMR spectra of the cardenolides digitoxigenin, digoxigenin, digitoxin, and mono- and bis-digitoxigenin digitoxosides have been completely assigned by two-dimensional NMR spectroscopy. The techniques used include phase-sensitive COSY, multiple relay COSY, and carbon–proton correlation (HETCOR and HMQC) spectra. Various aspects of the solution conformation of the steroid moiety of digitoxin and digoxigenin could be determined from coupling constants and NOE difference experiments and they are indicative of an all-chair conformation. The carbohydrate rings in digitoxin and the mono- and bis-digitoxigenin digitoxosides are also in the chair conformation. Keywords: cardenolides, digitoxigenin, digitoxin, 2-dimensional NMR, conformational analysis.


1990 ◽  
Vol 53 (6) ◽  
pp. 1456-1462 ◽  
Author(s):  
Jaume Bastida ◽  
Carles Codina ◽  
Francesc Viladomat ◽  
Mario Rubiralta ◽  
Jean-Charles Quirion ◽  
...  

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