## Abstract The role of steric factors in magnetic non‐equivalence anisochronism of complex geminal groups and of their fragments in compounds of the general formula RCH(Ph)CH(COOR′)~2~ has been investigated. CMR anisochronism is more sensitive to conformational and other steric changes than is PMR
Some aspects of anisochronism of geminal methyl groups in quaternised α-dimethylamino esters (1H and 13C NMR)
✍ Scribed by Janusz Da̧browski; Andrzej Ejchart; Krystyna Kamieńska-Trela
- Publisher
- John Wiley and Sons
- Year
- 1973
- Tongue
- English
- Weight
- 376 KB
- Volume
- 5
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
The magnitude of chemical shift nonequivalence (Δδ) in compounds having the general formula R^1^CH(COOR^2^)N^+^R^3^Me~2~X^−^ is discussed from the viewpoint of selective shielding of one of the geminal groups by the ester group in the preferred rotamer. In addition, a novel example of the increase of Δδ with rise in temperature has been observed.
📜 SIMILAR VOLUMES
## Abstract The complete assignments of the ^1^H and ^13^C NMR spectra of the some α‐arylthio and α‐arylsulfonyl substituted __N__‐methoxy‐__N__‐methyl propionamides, bearing methoxy, methyl, chloro, and nitro as substituents at the phenyl ring are reported. Copyright © 2006 John Wiley & Sons, Ltd.
To determine the proportion of isolated methyl groups (i.e. methyl groups attached to hydrogen-free carbon) in a ground water humic substance (HS), four different techniques were applied: the standard proton spin-echo technique, the 'H-INADEQUATE method, a short version of the latter with a 4 4 puls