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17O NMR study of steric hindrance in methoxylated flavones. Substitution on the phenyl ring and the heterocycle

✍ Scribed by Jean-Claude Wallet; Emile M. Gaydou; M. T. Cung


Publisher
John Wiley and Sons
Year
1990
Tongue
English
Weight
212 KB
Volume
28
Category
Article
ISSN
0749-1581

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✦ Synopsis


Abstract

Natural abundance ^17^O NMR spectra were recorded for ten methoxyflavones and one flavonol. The chemical shifts are discussed in terms of steric and conformational changes. They are related to previously reported ^13^C NMR data.


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