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Selective HOESY experiments for stereochemical determinations

Identifieur interne : 002377 ( Istex/Curation ); précédent : 002376; suivant : 002378

Selective HOESY experiments for stereochemical determinations

Auteurs : Mehdi Yemloul [France] ; Sabine Bouguet-Bonnet [France] ; Lalla Aïcha Ba [France] ; Gilbert Kirsch [France] ; Daniel Canet [France]

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RBID : ISTEX:9A859BC5C921B33DC30B5E2EF39231149069D04B

English descriptors

Abstract

Heteronuclear Overhauser effect spectroscopy (HOESY) is a powerful method for tracking geometrical proximities between two heteronuclei (for instance, 1H and 13C, as this will be the case here). The method is based on cross‐relaxation arising from dipolar interactions. Sensitivity permitting, it is applied in the 2D mode yielding all spatial correlations in a single experiment. Whenever sensitivity is not sufficient, it can be applied in the one‐dimensional mode by selectively inverting one particular proton. In that case, it yields, from the carbon‐13 spectrum, remote spatial correlations. The method has been employed here for the discrimination between two possible E or Z isomers in a medium‐size molecule. Copyright © 2008 John Wiley & Sons, Ltd.

Url:
DOI: 10.1002/mrc.2283

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ISTEX:9A859BC5C921B33DC30B5E2EF39231149069D04B

Le document en format XML

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<term>Dante pulse train</term>
<term>Dipolar interactions</term>
<term>Equilibrium magnetization</term>
<term>Experimental data</term>
<term>Experimental methods</term>
<term>Heteronuclear overhauser effect spectroscopy</term>
<term>Hoesy</term>
<term>Independent measurements</term>
<term>Initial slope</term>
<term>Interatomic</term>
<term>Interatomic distances</term>
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<term>Nuclear overhauser effect</term>
<term>Phase cycle</term>
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<term>Relaxation rates</term>
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<term>Remote carbons</term>
<term>Reson</term>
<term>Selective experiment</term>
<term>Selective hoesy experiments</term>
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<div type="abstract" xml:lang="en">Heteronuclear Overhauser effect spectroscopy (HOESY) is a powerful method for tracking geometrical proximities between two heteronuclei (for instance, 1H and 13C, as this will be the case here). The method is based on cross‐relaxation arising from dipolar interactions. Sensitivity permitting, it is applied in the 2D mode yielding all spatial correlations in a single experiment. Whenever sensitivity is not sufficient, it can be applied in the one‐dimensional mode by selectively inverting one particular proton. In that case, it yields, from the carbon‐13 spectrum, remote spatial correlations. The method has been employed here for the discrimination between two possible E or Z isomers in a medium‐size molecule. Copyright © 2008 John Wiley & Sons, Ltd.</div>
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