## 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 stru
Conformational analysis: IX–a 300 MHz study of 4-vinylbutyrolactone
✍ Scribed by Kalevi Pihlaja; Frank G. Riddell; Jorma Jalonen; Pirkko Rinta-Panttila; Marc Anteunis
- Publisher
- John Wiley and Sons
- Year
- 1974
- Tongue
- English
- Weight
- 205 KB
- Volume
- 6
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The 300 MHz ^1^H NMR spectrum of 4‐vinylbutyrolactone has been recorded and analysed. The results showed that the compound is a mixture of two rapidly interconverting envelope forms in which (C‐3) is the flap atom. The vinyl group favours the pseudo‐equatorial orientation by 1·9 ± 0.3 kJ mol^−1^, as shown by the dependence of the vicinal coupling constants on temperature.
📜 SIMILAR VOLUMES
## Abstract NMR spectra of __cis__‐ and __trans__‐2‐methyl‐4‐halogeno‐methyl‐1,3‐dioxolanes have been analysed at 300 MHz. Some of the extracted parameters facilitate easy distinction between these 1,3‐dioxolanes and the corresponding structurally isomeric 2‐Methyl‐5‐halogeno‐1,3‐dioxanes. Criteria
Some 2-alkyl-4-methyl-2,6-diphenyl-2H-thiopyrans were synthesized, and the crystal structure of 2-tert-butyl-4-methyl-2,6-diphenyl-2Hthiopyran 1 was determined by single-crystal X-ray diffraction. X-ray crystallographic analysis and ab initio HF/6-31G(d) and B3LYP/6-31G(d) calculations revealed a fa
## Abstract The synthesis of a D/E __cis__ isomer of the title compound is described. In an attempt to obtain the other D/E __cis__ isomer, epimerisation reactions were studied. The configuration and conformation of the isomers are determined on the basis of their ^1^H NMR spectra. The shift of the