## Abstract The signs of all ^13^C^19^F and ^1^H–^19^F coupling constants in fluorobenzene, some substituted derivatives, and in 2‐fluoropyridine have been related using single‐frequency ^13^C{^1^H} double resonance techniques. All ^13^C^19^F couplings in these compounds are shown to be positive
Indirect 1H19F1H and 1H19F13C nuclear overhauser enhancements: Anomalous intensity effects and applications in conformational analysis
✍ Scribed by Francisco Sánchez-Ferrando; Jeremy K. M. Sanders
- Publisher
- John Wiley and Sons
- Year
- 1987
- Tongue
- English
- Weight
- 389 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Indirect nuclear Overhauser enhancements through 19F have been determined for the three-spin systems 'H-I9F-'H and 1H-'9F-'3C by steady-state presaturation of the appropriate proton, and applied to the conformational analysis of 5-bromo-2-fluoro-4-nitroacetanilide. The 'H NOE difference spectra at 400 MHz showed antiphase doublets for protons undergoing simultaneous dipolar relaxation with, and scalar coupling to, I9F. Similarly, in the 13C selective NOE difference spectrum at 100 MHz, the two lines of the fluorine-bearing carbon showed negative enhancement factors of different magnitude on presaturation of the appropriate proton. The use of these anomalous intensity effects in conformational analysis is illustrated.
📜 SIMILAR VOLUMES
The cis/trans conformational equilibrium of the two Ac-Pro isomers of the beta-turn model dipeptide [13C]-Ac-L-Pro-D-Ala-NHMe, 98% 13C enriched at the acetyl carbonyl atom, was investigated by the use of variable temperature gradient enhanced 1H-nmr, two-dimensional (2D) 1H,1H nuclear Overhauser eff
## Abstract Chemical shift assignment of seven __N__‐substituted 6‐(4‐methoxyphenyl)‐7__H__‐pyrrolo[2, 3‐__d__]pyrimidin‐4‐amines, six of which are fluorinated, have been performed based on ^1^H, ^13^C, ^19^F, and 2D COSY, HMBC and HSQC experiments. Copyright © 2009 John Wiley & Sons, Ltd.