Solution conformational study of Scyliorhinin I analogues with conformational constraints by two-dimensional NMR and theoretical conformational analysis

2000 ◽  
Vol 56 (3) ◽  
pp. 132-146 ◽  
Author(s):  
S. Rodziewicz-Motowidło ◽  
A. Łegowska ◽  
X.-F. Qi ◽  
C. Czaplewski ◽  
A. Liwo ◽  
...  
1990 ◽  
Vol 68 (7) ◽  
pp. 1238-1250 ◽  
Author(s):  
Grigory M. Lipkind ◽  
Nikolay E. Nifant'ev ◽  
Alexander S. Shashkov ◽  
Nikolay K. Kochetkov

1H and 13C NMR spectra have been recorded and the nuclear Overhauser enhancements (in D2O), after pre-irradiation of the anomeric protons, have been measured for tri- and tetrasaccharides containing 2,3-disubstituted residues of α-L-rhamnose and the corresponding disaccharides. The proximity of the conformational states of the disaccharide units in these branched oligosaccharides and in the corresponding disaccharides has been shown, on the basis of both the nOe experimental data and theoretical conformational analysis. This conclusion is also confirmed by data for glycosylation effects in the 13C NMR spectra of the oligosaccharides. Keywords: branched oligosaccharides, 1H and 13C NMR spectra, conformations.


1975 ◽  
Vol 11 (2) ◽  
pp. 217-222
Author(s):  
I. S. Maksumov ◽  
S. F. Arkhipova ◽  
G. M. Lipkind ◽  
E. M. Popov

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