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Gradient heteronuclear multiple quantum correlation

The first of the proton-detected experiments is the Heteronuclear Multiple Quantum Correlation HMQC experiment of Bax, Griffey and Hawkins reported in 1983, which was first demonstrated using 1H-15N heteronuclear shift correlation [42]. The version that has come into wide-spread usage, particularly among the natural products community, is that of Bax and Subramanian reported in 1986 [43]. A more contemporary gradient-enhanced version of the experiment is shown in Fig. 10.14 [44],... [Pg.292]

In the heteronuclear experiment category, the experiments of interest are the heteronuclear multiple quantum correlation (HMQC) experiment, the heteronuclear single quantum correlation (HSQC) experiment, and the heteronuclear multiple bond correlation (HMBC, including the gradient-selected version gHMBC) experiment. Both the HMQC and HSQC produce similar results, but each has its own unique advantages and disadvantages. [Pg.124]

Fig. 10.14. Gradient-enhanced HMQC pulse sequence described in 1991 by Hurd and John derived from the earlier non-gradient experiment of Bax and Subramanian. For 1H-13C heteronuclear shift correlation, the gradient ratio, G1 G2 G3 should be 2 2 1 or a comparable ratio. The pulses sequence creates heteronuclear multiple quantum of orders zero and two with the application of the 90° 13C pulse. The multiple quantum coherence evolves during the first half of ti. The 180° proton pulse midway through the evolution period decouples proton chemical shift evolution and interchanges the zero and double quantum coherence terms. Antiphase proton magnetization is created by the second 90° 13C pulse that is refocused during the interval A prior to detection and the application of broadband X-decoupling. Fig. 10.14. Gradient-enhanced HMQC pulse sequence described in 1991 by Hurd and John derived from the earlier non-gradient experiment of Bax and Subramanian. For 1H-13C heteronuclear shift correlation, the gradient ratio, G1 G2 G3 should be 2 2 1 or a comparable ratio. The pulses sequence creates heteronuclear multiple quantum of orders zero and two with the application of the 90° 13C pulse. The multiple quantum coherence evolves during the first half of ti. The 180° proton pulse midway through the evolution period decouples proton chemical shift evolution and interchanges the zero and double quantum coherence terms. Antiphase proton magnetization is created by the second 90° 13C pulse that is refocused during the interval A prior to detection and the application of broadband X-decoupling.
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]

Fig. 10.15. Pulse sequence for the multiplicity-edited gradient HSQC experiment. Heteronuclear single quantum coherence is created by the first INEPT step within the pulse sequence, followed by the evolution period, t . Following evolution, the heteronuclear single quantum coherence is reconverted to observable proton magnetization by the reverse INEPT step. The simultaneous 180° XH and 13C pulses flanked by the delays, A = l/2( 1 edits magnetization inverting signals for methylene resonances, while leaving methine and methyl signals with positive phase (Fig. 16A). Eliminating this pulse sequence element affords a heteronuclear shift correlation experiment in which all resonances have the same phase (Fig. 16B). Fig. 10.15. Pulse sequence for the multiplicity-edited gradient HSQC experiment. Heteronuclear single quantum coherence is created by the first INEPT step within the pulse sequence, followed by the evolution period, t . Following evolution, the heteronuclear single quantum coherence is reconverted to observable proton magnetization by the reverse INEPT step. The simultaneous 180° XH and 13C pulses flanked by the delays, A = l/2( 1 edits magnetization inverting signals for methylene resonances, while leaving methine and methyl signals with positive phase (Fig. 16A). Eliminating this pulse sequence element affords a heteronuclear shift correlation experiment in which all resonances have the same phase (Fig. 16B).
More recently, a gradient-enhanced heteronuclear single quantum multiple bond correlation (HSQMBC) experiment and its variants34,47,60-62 have been proposed for the measurement of heteronuclear coupling... [Pg.200]

The inverse-detected 2D NMR experiments that have been discussed to this point have all been discrete, single-purpose experiments, e.g. correlating protons with their directly bound heteronucHde (typically or N). There are another class of inverse-detected 2D NMR experiments that are generally referred to as hyphenated 2D experiments. These are experiments that first establish one type of correlation, followed by an additional experiment segment that then pursues a further spectroscopic task. Predecessors of the inverse-detected variants of these experiments were the HC-RELAY (proton—carbon heteronuclear relayed coherence transfer) experiments pioneered by Bolton [151—155]. Examples of these include, but are by no means hmited to HXQC-COSY and -TOCSY [156—158], -NOESY [159], -ROESY [160], and more recent gradient variants [161] etc., where X = S (single) or M (multiple) quantum variants of the experiments. [Pg.252]


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Gradient correlation

Gradient heteronuclear multiple

Gradient heteronuclear multiple quantum

Heteronuclear correlations

Heteronuclear multiple quantum correlation

Heteronuclear multiple-quantum

Multiple correlation

Multiple heteronuclear

Quantum correlations

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