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Heteronuclear single quantum resonance assignment

Traditionally, homonuclear 2D double quantum filtered correlation spectroscopy (DQF-COSY) and total correlated spectroscopy (TOCSY) spectra are valuable in the identification of resonances of individual monosaccharide units. In the presence of small couplings, through space connectivities detected by NOESY/ROESY (nuclear Overhauser effect spectroscopy/ rotational nuclear Overhauser effect spectroscopy) experiments are also useful in completing the resonance assignment. When the H NMR spectra of complex oligosaccharides are too crowded to fully elucidate the structure by homonuclear correlation methods, it is efficient to use 2D heteronuclear correlation methods, such as heteronuclear single quantum correlation... [Pg.198]

The final step in the assignment of all resonances is correlating the C peaks with the proton peaks. This can often be done from chemical shift alone for the anomeric resonances, but not for other ring atoms. The most important pulse sequence here is HSQC (Heteronuclear Single Quantum Correlation), which involves six pulses to protons and four to C. The spectrum is now a non-symmetrical map with a peak at each carbon attached to a proton the projection on the C axis is the C DEPT spectrum and on the proton axis the ordinary proton spectrum (Figure 4.18). [Pg.165]


See other pages where Heteronuclear single quantum resonance assignment is mentioned: [Pg.182]    [Pg.181]    [Pg.443]    [Pg.119]    [Pg.249]    [Pg.435]    [Pg.437]    [Pg.296]    [Pg.255]    [Pg.560]    [Pg.192]    [Pg.109]    [Pg.45]    [Pg.484]   


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