## Abstract The additive behaviour generally observed for the substituent‐induced chemical shifts (SCS) for disubstituted benzenes was examined for a series of aryl 2‐__N__‐acetamido‐2‐deoxy‐β‐D‐glucopyranosides having a wide range of __para__ substituents with varying possible electronic contribut
1H and 13C chemical shift assignments of para-substituted aryl 2-acetamido-2-deoxy-β-D-glucopyranosides
✍ Scribed by René Roy; François D. Tropper; Antony J. Williams
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 302 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
The ^1^H and ^13^C NMR spectra of twenty aryl 2‐acetamido‐2‐deoxy‐β‐D‐glucopyranosides and eighteen aryl 3,4,6‐tri‐O‐acetyl‐2‐acetamido‐2‐deoxy‐β‐D‐glucopyranosides have been obtained and assigned. The three‐bond proton coupling constants of these compounds were also obtained.
📜 SIMILAR VOLUMES
The 1H and 13C NMR resonances of four 3H-naphtho[2,1-b]pyrans were completely and unambiguously assigned by a combination of homonuclear (gs-COSY), 1H-detected heteronuclear one-bond (gs-HMQC) and long-range (gs-HMBC) gradient-selected correlation experiments.
## Abstract The proton and carbon spectra of new 2,4‐diaryl‐substituted cycloalkyl[__d__]pyrimidines prepared in a simple one‐pot reaction, are reported. Copyright © 2002 John Wiley & Sons, Ltd.