The determination of aromatic substitution patterns by nuclear magnetic resonance
β Scribed by M. Zanger
- Publisher
- John Wiley and Sons
- Year
- 1972
- Tongue
- English
- Weight
- 996 KB
- Volume
- 4
- Category
- Article
- ISSN
- 0749-1581
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β¦ Synopsis
A method is described which permits the analysis of many substituted benzene compounds. The method is useful for mono-through tetra-substituted aromatics. In ideal cases, the number and disposition of the substituents and the chemical shifts of the residual protons can be accurately determined. The method assumes approximate first order couplings and is useful for roughly 50 % of all aromatics. Frequently observed anomalous spectra are also discussed. 1 1 -0.50 -0.43 -0.75 +0.18 -0.06 -0.13 -0.27 +0-17 +@14 -1-0.07 -0.14 -0.09 -0.24 -0.06 -0.04 -0.03 -0.07 +0-33 +0.2 + 0.02 -0.4 -0.37 -0.63 -0.06 a All other values were taken from Ref. 2.
π SIMILAR VOLUMES
Determination of whether CO2 or HCO3- is the substrate for an enzymatic carboxylation has generally been accomplished by taking advantage of the fact that equilibration of these two compounds requires more than a minute at temperatures below 15 degrees C; thus different kinetics of carboxylation are
## Abstract A series of __m__β and __p__βsubstituted anilides of benzoic acid, 2βthienoic acid, and 2βfuroic acid were prepared and their ^1^H and ^13^C nmr spectroscopic characteristics were examined. In general, good correlations were observed between the chemical shifts of proton and carbon sign