## Abstract The ^15^N chemical shifts of aniline, the toluidines, xylidines, and several halogen and oxygen substituted anilines have been measured at the natural abundance level of ^15^N. Substituent parameters obtained by multiple regression analysis show that the methyl group induces comparable
Nitrogen-15 nuclear magnetic resonance spectroscopy. Natural abundance nitrogen-15 spectra of the cis and trans isomers of secondary alkylformamides
✍ Scribed by Hiroshi Nakanishi; John D. Roberts
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- English
- Weight
- 577 KB
- Volume
- 15
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
The ^15^NMR chemical shifts were measured of a number of N‐substituted formamides and acetamides at the natural abundance level. The ratios of the cis and trans isomers for several N‐alkylformamides were also determined. Substituent effects on the ^15^N chemical shifts of formamides are compared with those of some other nitrogen‐containing compounds. There is a consistent pattern of behavior of the one bond spin–spin coupling constants [^1^J(^15^NH)] wherein the trans isomers of N‐alkylformamides are larger than those of the cis isomers.
📜 SIMILAR VOLUMES
## 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