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Synthesis, stereochemistry, and isomeric transformations of cis- and trans-1,2-dimethyl-4-aryl-5-aroyl-2-imidazolines

✍ Scribed by I. G. Tishchenko; O. N. Bubel'; V. A. Konovalov

Book ID
112348793
Publisher
Springer US
Year
1981
Tongue
English
Weight
663 KB
Volume
17
Category
Article
ISSN
0009-3122

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1H NMR spectra and stereochemistry of ci
1H NMR spectra and stereochemistry of cis- and trans-5,6-dimethyl-2-oxo-1,4-dioxans
✍ Pertti Γ„yrΓ€s πŸ“‚ Article πŸ“… 1975 πŸ› John Wiley and Sons 🌐 English βš– 203 KB

## Abstract The ^1^H NMR spectra of isomeric 5,6‐dimethyl‐2‐oxo‐1,4‐dioxans have been recorded and the pertinent chemical shifts and coupling constants determined. The parameters indicate that both isomers exist as an equilibrium mixture of interconverting half chair ring conformations.