Application of homonuclear and heteronuclear two-dimensional chemical-shift correlation NMR spectroscopy to the complete assignment of proton and carbon-13 NMR spectra of ionophorous antibiotic X.14547 A

1984 ◽  
Vol 49 (10) ◽  
pp. 1797-1800 ◽  
Author(s):  
J. C. Beloeil ◽  
M. A. Delsuc ◽  
J. Y. Lallemand ◽  
G. Dauphin ◽  
G. Jeminet



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


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.



1982 ◽  
Vol 123 (1) ◽  
pp. 127-131 ◽  
Author(s):  
Nigel J. CLAYDEN ◽  
Fuyuhiko INAGAKI ◽  
Robert J. P. WILLIAMS ◽  
Gareth A. MORRIS ◽  
Kazuo TORI ◽  
...  


1988 ◽  
Vol 43 (8) ◽  
pp. 1072-1074 ◽  
Author(s):  
Bruno Perly ◽  
Giuseppe C. Pappalardo ◽  
Michael Klaus ◽  
Enzo Montoneri

AbstractThe 1H NMR spectra (in DMSO solution at 300 K) of retinoic acids (cis- and trans-isomers) and new arotinoids were run at 500 MHz and assigned by using homo- and heteronuclear two-dimensional (2D) chemical shift correlation experiments. Spectral analysis was indicating, on the basis of 7 values, that the ring C(l)-C(2)-C(3)-C(4)-C(5)-C(6) adopts, in all compounds, a chair conformation.



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