The =C chemical shifts of a series of isoflavones having hydroxy, acetoxy, methoxy and methylenedioxy substituents are compared. Some general relationships between substitution patterns and chemical shifts, useful for the identitication of naturally occurring isoflavones, are outlined.
The carbon-13 nuclear magnetic resonance spectra of anthraquinone, eight polyhydroxyanthraquinones and eight polymethoxyanthraquinones
✍ Scribed by Y. Berger; A. Castonguay
- Publisher
- John Wiley and Sons
- Year
- 1978
- Tongue
- English
- Weight
- 271 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
The ^13^C NMR spectra of anthraquinone, eight hydroxyanthraquinones and eight methoxyanthraquinones are reported. Peak assignment for the carbon atoms of these compounds is achieved by using decoupling techniques and by intercomparison of the variously‐substituted derivatives. Carbonyl chemical shifts in the hydroxyanthraquinones can be rationalized in terms of cross conjugation and intramolecular hydrogen bonding and in terms of cross conjugation in the methoxyanthraquinones. Hydroxy and methoxy substituent chemical shifts are also reported.
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