## Abstract The relative acidities of the __cis__ and __trans__ isomers of a series of 1,5‐oxazaspiro[5.5]undecane derivatives were determined by measuring Δp__K__ in acid‐base titrations followed by ^1^ H NMR. Relative structural stabilities were determined by measuring substituent chemical shift
Identification of 2-chloropyrazine oxidation products and several derivatives by multinuclear magnetic resonance
✍ Scribed by Piotr Cmoch
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 124 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.1232
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
^1^H, ^13^C, ^14^N and ^15^N NMR chemical shifts were used to prove the structures of the products of 2‐chloropyrazine oxidation. It was shown that oxidation by hydrogen peroxide in acetic acid or m‐chloroperbenzoic acid leads to the __N__4‐oxide, whereas potassium persulfate in sulfuric acid gives the __N__1‐oxide as the main product. Additionally, the results of NMR measurements of products from the nucleophilic substitution of the chlorine atom by azide anion, yielding the respective azides, and ethylation reactions of both 2‐chloropyrazine N‐oxides leading to the N‐ethyl salts confirm the structures of both isomeric N‐oxides. Protonation studies of the compounds obtained are also reported. The favoured protonation site is found to be the N atom that is not hindered by any substituents, and in some cases probably the oxygen atom of the N‐oxide function. Copyright © 2003 John Wiley & Sons, Ltd.
📜 SIMILAR VOLUMES
## Note Identification of the products of periodate oxidation of some mono-Oisopropylidene derivatives of aldoses and alditols by g.l.c.-m.s.
## Abstract Enantiomeric ratios of compounds with P=Se functionalities (phosphine selenides) can easily be determined by ^1^H, ^13^C, ^31^P, and ^77^Se NMR spectroscopic inspection of their diastereomeric complexes with (__R__)‐Rh~2~(MTPA)~4~ (MTPA‐H ≡ methoxytrifluoromethylphenylacetic acid; Moshe
## Abstract Absolute coupling signs of ^1^__J__(^119^Sn, ^13^C) (2__J__(^119^Sn, ^1^H) (n^5^‐C~5~H~5~)~2~Sn (1) and ^1^__J__(^119^Sn, ^13^C) (2__J__(^119^Sn, ^13^C) (3__J__(^119^Sn, ^1^H) (>O) in (__n__^5^‐C~5~Me~5~)~2~Sn (2) were determined using advanced direct and indirect two‐dimensional method
## Abstract Two series of 2,5‐diaryl‐1,3,4‐oxadiazolines have been studied by multinuclear magnetic resonance and density functional theory calculations. A full NMR spectroscopic characterization has been performed and excellent remote Hammett correlations (σ~p~ or $\sigma\_{\rm {p}}^{+}$) have bee