𝔖 Bobbio Scriptorium
✦   LIBER   ✦

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

No coin nor oath required. For personal study only.

✦ 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.


📜 SIMILAR VOLUMES


Nitrogen-15 nuclear magnetic resonance s
✍ Karl Eberl; John D. Roberts 📂 Article 📅 1981 🏛 John Wiley and Sons 🌐 English ⚖ 173 KB 👁 1 views

## 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

Nitrogen-15 nuclear magnetic resonance s
✍ Issa Yavari; John S. Staral; John D. Roberts 📂 Article 📅 1979 🏛 John Wiley and Sons 🌐 English ⚖ 257 KB

## Abstract The ^15^N NMR spectra of ten isocyanates, four isothiocyanates, and four __N__‐sulfinylamines have been obtained at the natural‐abundance level by high‐resolution NMR spectroscopy. The results show that isocyanates and isothiocyanates have ^15^N chemical shifts over 200 ppm toward highe

15N nuclear magnetic resonance spectrosc
✍ Robert E. Botto; Philip W. Westerman; John D. Roberts 📂 Article 📅 1978 🏛 John Wiley and Sons 🌐 English ⚖ 560 KB

## Abstract ^15^N chemical shifts of the __Z__ and __E__ isomers of twenty‐two ketoximes and fourteen aldoximes have been determined at the natural‐abundance level of ^15^N, using Fourier transform methods. The influences of π delocalization, methyl substituents and solute concentration on the oxim

Nitrogen-15 nuclear magnetic resonance s
✍ Issa Yavari; John D. Roberts 📂 Article 📅 1979 🏛 John Wiley and Sons 🌐 English ⚖ 545 KB

## Abstract The noise‐decoupled nitrogen‐15 NMR spectra of ten pyridine __N__‐oxides and two quinoline __N__‐oxides have been obtained at the natural‐abundance level by high‐resolution NMR spectroscopy. Substituents at the 4‐ring position of pyridine __N__‐oxide, capable of resonance interaction wi

Nitrogen-15 nuclear magnetic resonance s
✍ Hiroshi Nakanishi; John D. Roberts 📂 Article 📅 1981 🏛 John Wiley and Sons 🌐 English ⚖ 577 KB

## 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 o