The 1 H and 13 C NMR spectra of seven 2-substituted phenyl methyl sulphides were measured and their chemical shifts assigned on the basis of two-dimensional NMR techniques such as H,H-COSY and C,H-COSY. The chemical shifts of these sulphides were correlated with the appropriate SCS values of monosub
Conformational analysis. XIII—A 300 MHz 1H NMR study of 2-methyl-, 2-phenyl-, 2-(2-chlorophenyl)-and 2-(4-chlorophenyl)-oxetanes
✍ Scribed by Kalevi Pihlaja; Jukka Jokisaari; P. Olavi; I. Virtanen; Heikki Ruotsalainen; Marc Anteunis
- Publisher
- John Wiley and Sons
- Year
- 1975
- Tongue
- English
- Weight
- 446 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
The 300 MHz spectra of 2‐methyl‐, 2‐phenyl‐, 2‐(2‐chlorophenyl)‐ and 2‐(4‐chlorophenyl)‐oxetanes were recorded in CCl~4~ and C~6~D~6~. The chemical shifts and the proton‐proton coupling constants were solved through iterative calculations. The results were discussed in the light of structural factors and theoretical calculations. The average angle of pucker for the oxetane ring was estimated at c. 5°, in fair agreement with the value of 3·3° derived from a microwave study.
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