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Use of1H and13C NMR spectroscopy to determine the stereochemistry of 1,4,5-trime thyl-4-cyclohexene-1,2-dicarboxylic acids and their derivatives

โœ Scribed by V. A. Denisenko; V. L. Novikov; V. V. Isakov; A. V. Kamernitskii; G. B. Elyakov


Book ID
112437300
Publisher
Springer
Year
1976
Tongue
English
Weight
224 KB
Volume
25
Category
Article
ISSN
1573-9171

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Assignment of the 1H and 13C NMR spectra
โœ Lyle W. Castle; Andrew S. Zektzer; Milton D. Johnston Jr. ๐Ÿ“‚ Article ๐Ÿ“… 1992 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 470 KB

## Abstract The ^1^H NMR spectrum of naphtho [1โ€ฒ,2โ€ฒ:4,5]thieno[2,3โ€__c__]quinoline is highly congested because all the protons are in an aromatic environment, and the structure of the molecule is nearly symmetric. With this in mind, the assignment of the ^1^H and ^13^C NMR spectra of this compound