ChemInform Abstract: AUTOCORRELATED CARBON-13-CARBON-12 DOUBLE QUANTUM COHERENCE TWO-DIMENSIONAL NMR SPECTROSCOPY: UTILIZATION OF A MODIFIED VERSION OF THE TECHNIQUE AS AN ADJUNCT IN THE TOTAL ASSIGNMENT OF THE PROTON AND CARBON-13 NMR SPECTRA OF THE MUTA

1984 ◽  
Vol 15 (28) ◽  
Author(s):  
M. J. MUSMAR ◽  
M. R. III WILLCOTT ◽  
G. E. MARTIN ◽  
R. T. JUN. GAMPE ◽  
M. 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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