## Abstract Nitrogen and carbon electron densities of the toluidines and xylidines have been recalculated by the INDO method; previously published errors have been corrected. Although the nitrogen‐15 chemical shifts of these compounds still display the earlier suggested correlation with σ and total
Nitrogen-15 nuclear magnetic resonance spectroscopy. Chemical shifts of methyl substituted cis-decahydroquinolines
✍ Scribed by Friedrich W. Vierhapper; George T. Furst; Robert L. Lichter
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- English
- Weight
- 446 KB
- Volume
- 17
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
^15^N Chemical shifts of cis‐decahydroquinoline, N‐methyl‐cis‐decahydroquinoline, and of 19 methyl substituted NH‐ and NCH~3~‐cis‐decahydroquinolines are reported. Shift values of conformationally homogeneous compounds can be used to determine the chemical shifts of the possible conformations of the mobile compounds. Equilibrium constants derived from the shifts of the contributing conformations agree with results of low temperature ^13^C NMR spectroscopy.
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