Sequential resonance assignments in proton NMR spectra of oligonucleotides by two-dimensional NMR spectroscopy

Biochemistry ◽  
1984 ◽  
Vol 23 (7) ◽  
pp. 1371-1376 ◽  
Author(s):  
R. M. Scheek ◽  
R. Boelens ◽  
N. Russo ◽  
J. H. Van Boom ◽  
R. Kaptein
1980 ◽  
Vol 58 (18) ◽  
pp. 1947-1956 ◽  
Author(s):  
Alex D. Bain ◽  
Russell A. Bell ◽  
Jeremy R. Everett ◽  
Donald W. Hughes

An alternative two-dimensional nmr pulse sequence, (90°–t1/2–90°–t1/2–FID),correlates the chemical shifts of coupled nuclei. The application of this technique to the solution of the complicated proton nmr spectra of oligoribonucleotides is discussed.


1983 ◽  
Vol 105 (9) ◽  
pp. 2914-2916 ◽  
Author(s):  
R. M. Scheek ◽  
N. Russo ◽  
R. Boelens ◽  
R. Kaptein ◽  
J. H. Van Boom

1983 ◽  
Vol 14 (32) ◽  
Author(s):  
R. M. SCHEEK ◽  
N. RUSSO ◽  
R. BOELENS ◽  
R. KAPTEIN ◽  
J. H. VAN BOOM

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.


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