## Abstract The ^1^H n.m.r. spectrum of 3‐methyl‐2‐oxo‐1,4‐dioxepane was recorded at 300 and 60 MHz. The ring conformation was considered in terms of the spectral parameters and shown to be a twisted boat where the lactone grouping is approximately planar.
Analysis of the 1H n.m.r. spectrum of 4-methyl-1,3-oxathiolane. An interestingly coupled ABXM3-case
✍ Scribed by Kalevi Pihlaja; Raimo Keskinen
- Publisher
- John Wiley and Sons
- Year
- 1977
- Tongue
- English
- Weight
- 176 KB
- Volume
- 9
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
The 220 MHz proton magnetic resonance spectrum of 4‐methyl‐1,3‐oxathiolane was recorded and analysed. The methyl and ethanic protons form an ABXM~3~ system, the analysis of which was carried out through several ‘trial‐and‐error’ attempts. This part of the spectrum is an interesting example of second‐order effects which, in the past, have been mistakenly associated with ‘virtual coupling’. The results are compared with those presented earlier for several alkyl substituted 4‐methyl‐1,3‐oxathiolanes.
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