## Abstract The free energy of the axial–equatorial equilibrium of 2‐methylcyclohexanone oxime (1E) and the corresponding __O__‐methyl oxime (2E) was determined by a novel curve‐fitting analysis of the temperature dependence of the carbon chemical shifts and by the vicinal proton–proton coupling co
Carbon-13 NMR study of enamines and enamino ketones. A direct observation of the conformation of the 2-methylcyclohexanone enamine tautomers
✍ Scribed by D. Tourwé; G. Van Binst; S. A. G. De Graaf; U. K. Pandit
- Publisher
- John Wiley and Sons
- Year
- 1975
- Tongue
- English
- Weight
- 704 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
The carbon‐13 spectra of a series of cyclohexanone, cyclopentanone and 2‐methylcyclohexanone enamines are reported. The influence of the amino component was studied in a series of enamino ketones. The spectra reflect the amount of p‐π overlap in the molecules and their conformation. Differences between 5‐and 6‐membered carbonyl components are evaluated.
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