## Abstract The proton chemical shifts are reported for monosubstituted naphthalenes, quinolines and quinoxalines. Together with literature data, these chemical shifts are compared with the parent compounds and substituent effects evaluated statistically. The effect of substituents parallels that i
Proton magnetic resonance studies of substituted 3,5-dimethylbenzenes: Influence of substituents on the methyl proton chemical shifts
✍ Scribed by Fadhil S. Kamounah; Ikbal. S. Al-Sheibani; Nazar L. Shibaldain; Salman R. Salman
- Publisher
- John Wiley and Sons
- Year
- 1985
- Tongue
- English
- Weight
- 294 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Proton NMR data for a number of l-.IZ-4-Y-3,5-dimethylbenzenc?s and l-X-2-Y-4-Z-3,5-dimethylbenzenc?s are presented. The proton chemical shifts of the methyl groups at positions 3 and 5 are mainly affected by the ring current effect of the snbstituents. Thii conclusion was strongly supported by the proton chemical shifts calculated using additivity rules.
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## Abstract The ^13^C NMR chemical shifts for 1,3‐dithiolane and 13 methyl substituted derivatives are reported. Substituent effects are derived and compared with those for cyclopentanes and 1,3‐dioxolanes. The magnitude and variety of the substituent effects are best explained with the aid of a ha
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