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ROESY rotating-frame nuclear Overhauser

Glc glucose ROESY rotating-frame nuclear Overhauser... [Pg.123]

ROESY, rotating frame nuclear Overhauser enhanced spectroscopy. [Pg.333]

In contrast, with axle 15 only one orientation is observed at low temperature, even after 70 days. The assignment of the orientation could be obtained by the observation of ROESY (rotating frame nuclear overhauser effect correlation spectroscopy) cross-peaks between C5H CD protons and the 3-methylpyridine site and, conversely, the C3H CD protons with the site containing the disubstituted pyridine. However, increasing the temperature to 343 K equilibration takes place and the two orientations become equally populated, showing that the observed selectivity had a kinetic origin. [Pg.271]

ROESY Rotating frame nuclear Overhauser effect spectroscopy... [Pg.3226]

ROESY rotating frame nuclear overhauser spectroscopy... [Pg.302]

The data from H NMR studies of 63, which included double quantum filtered phase sensitive correlated spectroscopy (DQF-COSY) and rotating frame nuclear Overhauser effect spectroscopy (ROESY) experiments (Figure 12), are collected in Table 17. [Pg.95]

Fattorusso and co-workers identified a component of wormwood called artar-borol. Correlation spectroscopy (COSY) and rotating frame nuclear overhauser effect spectroscopy (ROESY) experiments allowed for deduction of four possible diastereomeric structures of artarborol, 2-5. Low energy conformers of 11-14 were obtained through a molecular mechanics (MM) search. These conformers were screened to identify those having a dihedral angle of around 90 for the C-8 and C-9 protons due to a low coupling constant between these protons. Only conformers of 11 and 13 satisfied this criterion. Next, five low energy conformers, two... [Pg.73]

The elucidation of the scalar coupling network by the correlation experiments is, apart from small molecules, not sufficient for the unambiguous, sequential and stereo-specific assignment. The complementary information of spatially adjacent protons is obtained via cross-relaxation experiments, the laboratory-frame nuclear Overhauser enhancement spectroscopy (NOESY) and the rotating-frame nuclear Overhauser effect spectroscopy (ROESY). These experiments provide also the distance restraints for the structure determination and help to recognize exchange processes. [Pg.708]

Rotating Frame Nuclear Overhauser Effect Spectroscopy (ROESY), NMR, a technique that allows exchange processes to be observed when applied to the trimethylam-monium salt of 12 in dichloromethane-rf2, provided evidence for aggregation in solution (Figure 14). Two resonances were observed between 7.0 and 7.5 ppm... [Pg.266]

Thus, as illustrated above, one-dimensional rotating frame nuclear Overhauser and exchange spectroscopy (ID-ROESY) experiments may provide a reasonable explanation for significant qualitative and quantitative differences observed in selector-selectand interactions related to chiral CE. This information becomes even... [Pg.135]

ROESY Rotating-frame Overhauser effect spectroscopy. A variation (one and two dimensional) on the nuclear Overhauser experiment (NOE). The techniques have the advantage of being applicable for all sizes of molecule. See Laboratory frame model. [Pg.209]

We described the basic aspects of NOESY in Section 10.1 as an introductory example of a 2D experiment. NOESY is very widely used in measuring macro-molecular conformation, as we see in Chapter 13. However, as shown in Fig. 8.4, the H— H nuclear Overhauser enhancement 17 varies from its value of +0.5 in small molecules to a limiting value of — 1 in large polymers with very long Tc, and at intermediate values of rc the NOE may vanish. An alternative is to use the NOE measured in the rotating frame, as this quantity is always positive. By analogy to NOESY, this technique has the acronym ROESY (rotating frame Overhauser enhancement spectroscopy),... [Pg.267]

NMR experiments include COSY, TOCSY, Cheteronuclear NMR experiments, NOESY (nuclear overhauser enhancement spectroscopy) and ROESY (rotating frame overhauser effect spectroscopy) as well as other two- and three-dimensional methodologies (Fossen and Andersen, 2006). [Pg.228]

NMR has become a standard tool for structure determination and, in particular, for these of Strychnos alkaloids. The last general article in this field was authored by J. Sapi and G. Massiot in 1994 [65] and described the advances in spectroscopic methods applied to these molecules. More recently, strychnine (1) has even been used to illustrate newly introduced experiments [66]. We comment, here, on their advantages and sum up the principles of usual 2D experiments in Fig. (1) and Fig. (2) (COSY Correlation SpectroscopY, TOCSY TOtal Correlation SpectroscopY, NOESY Nuclear Overhauser Enhancement SpectroscopY, ROESY Rotating frame Overhauser Enhancement SpectroscopY, HMQC Heteronuclear Multiple Quantum Coherrence, HMBC Heteronuclear Multiple Bond Correlation). This section updates two areas of research in the field new H and 13C NMR experiments with gradient selection or/and selective pulses, 15N NMR, and microspectroscopy. To take these data into account, another section comments on the structure elucidation of new compounds isolated from Strychnos. It covers the literature from 1994 to early 2000. [Pg.1040]

Heteronuclear Multiple Quantum Correlation) and HMBC (Heteronuclear Multiple Bond Correlation). Application of nuclear Overhauser effect (nOe) difference spectroscopy and nuclear Overhauser effect spectroscopy (NOESY) complete the analysis, giving atomic spatial relationships. Sensitivity problems can be alleviated using Homo Hartmann-Hahn spectroscopy (HOHAHA or TOCSY, Total Correlation Spectroscopy). For weak nOes a rotating frame experiment, i.e. ROESY (Rotating frame Overhauser Effect Spectroscopy) is useful, and may be the best experimental method to sequence chains of sugars [5]. [Pg.138]

ID, one-dimensional 2D, two-dimensional NOE, nuclear Overhauser effect ROESY, rotating-frame spectroscopy... [Pg.248]

FLZ fluconazole CD cyclodextrin P-CD P-cyclodextrin IH NMR proton Nucleic Magnetic Resonance spectroscopy 2D two dimensional COSY correlation SpectroscopY ROESY Rotating frame Overhauser Effect Spectros-copY NOE Nuclear Overhauser Effect [FI] host [Gj guest MOE Molecular Operating Environment. [Pg.180]


See other pages where ROESY rotating-frame nuclear Overhauser is mentioned: [Pg.1274]    [Pg.93]    [Pg.1485]    [Pg.1274]    [Pg.93]    [Pg.1485]    [Pg.408]    [Pg.211]    [Pg.175]    [Pg.414]    [Pg.94]    [Pg.45]    [Pg.156]    [Pg.287]    [Pg.173]    [Pg.156]    [Pg.491]    [Pg.18]    [Pg.168]    [Pg.653]    [Pg.348]    [Pg.1569]    [Pg.210]    [Pg.552]    [Pg.740]    [Pg.47]   


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Rotating frame nuclear Overhauser

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