## Abstract Nitrogen‐15 NMR spectra of 11 ketenimines have been taken both at the natural‐abundance level of ^15^N and with the aid of ^15^N‐labeling. The nitrogen chemical shifts are substantially different from those of neutral imines and are upfield, more like those of protonated imines. The res
N-Nitrosodecahydroquinolines 3-Nitrogen-15 Nuclear Magnetic Resonance Spectra
✍ Scribed by Friedrich W. Vierhapper; Puliyur R. Srinivasan
- Publisher
- John Wiley and Sons
- Year
- 1982
- Tongue
- English
- Weight
- 559 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
^15^N Chemical shifts of N‐nitroso‐trans‐decahydroquinoline, N‐nitroso‐cis‐decahydroquinoline, of 12 methyl‐or t‐butyl‐substituted N‐nitrosodecahydroquinolines and of N‐nitroso‐trans‐syn‐trans‐perhydroacridine are reported. Shift effects for N‐nitrosation were calculated by comparison with the parent amines. Shift effects for ring substitution, obtained by comparison with the data of N‐nitrosopiperidine, are of similar direction and magnitude as in the parent amines for the ring nitrogens (N‐1). Methyl substitution nearly always causes deshielding for the nitroso nitrogens (N‐2), with a very large deshielding if the planarity of the (C‐α)~2~NNO region is disturbed.
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