## Abstract Proton coupled carbon‐13 NMR spectra of eleven mono‐, di‐ and trimethylpyridines were analysed on a first order basis. The long range ^13^C^1^H coupling constants are similar to those observed for pyridine and cyanopyridines.
Long-range 13C1H coupling constants in 3-carene and α-pinene
✍ Scribed by Aleksej Y. U. Denisov; Evgenij A. Tyshchishin; Aleksej V. Tkachev; Viktor I. Mamatyuk
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- English
- Weight
- 433 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
Long‐range ^13^C^1^H coupling constants exceeding 0.3 Hz were measured for the hydrocarbons 3‐carene and α‐pinene by a heteronuclear 2D J‐resolved proton‐flip experiment with selective proton excitation. The dependences of the vicinal ^3^J(C, H) coupling constants on the dihedral angles were studied, and the peculiarities of the couplings through the double bond and cyclopropane framework were demonstrated. The dependences of the ^4^J(C, H) coupling constants in the allylic fragments of the molecular framework are discussed, and the long‐range ^n^J(C, H) coupling constants with the olefinic protons in camphene were investigated for the same purpose.
📜 SIMILAR VOLUMES
## Abstract One bond and long range ^13^C^1^H coupling constants for some methoxy‐, amino‐ and hydroxypyridines are described. An unambiguous assignment of carbon‐13 resonances is carried out based on the analysis of the fine splitting caused by long range couplings. __J__ values for compounds oth
## Abstract Chemical shifts and long‐range ^13^C, ^1^H coupling constants to the two carbonyl C atoms were determined for a series of ethyl 2‐acyloxy‐2‐alkenoates. The ^3^__J__(C,H) coupling constant across the double bond is 9.5–10.1 Hz for the __E__‐ and 2.9–3.8 Hz for the __Z__‐isomer. ^3^__J__(
## Abstract Long range ^13^C^1^H coupling constants are reported for a number of methylquinoline derivatives. The results have been compared with those observed in the pyridine series and correlated with ^1^H^1^H coupling constants.
In recent years, heteronuclear J cross-polarization experi-pled proton(s) via 1 H-1 H NOE when the source carbon is ments have been revitalized as a preferable alternative to protonated (13). Both selective one-dimensional and nonsetechniques based on pulse-interrupted free precession to lective mul